US10499813B2 - Methods, systems and apparatus for temporal calibration of an intravascular imaging system - Google Patents

Methods, systems and apparatus for temporal calibration of an intravascular imaging system Download PDF

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US10499813B2
US10499813B2 US14/484,832 US201414484832A US10499813B2 US 10499813 B2 US10499813 B2 US 10499813B2 US 201414484832 A US201414484832 A US 201414484832A US 10499813 B2 US10499813 B2 US 10499813B2
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Desmond Adler
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LightLab Imaging Inc
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Definitions

  • the disclosure relates generally to the field of vascular system and peripheral vascular system imaging and data collection.
  • Interventional cardiologists incorporate a variety of diagnostic tools during catheterization procedures in order to plan, guide, and assess therapies.
  • Fluoroscopy is generally used to perform angiographic imaging of blood vessels.
  • blood vessel imaging is used by physicians to diagnose, locate and treat blood vessel disease during interventions such as bypass surgery or stent placement.
  • Intravascular imaging technologies such as optical coherence tomography (OCT) and acoustic technologies such as intravascular ultrasound (IVUS) and others are also valuable tools that can be used in lieu of or in combination with fluoroscopy to obtain high-resolution data regarding the condition of the blood vessels for a given subject.
  • OCT optical coherence tomography
  • IVUS intravascular ultrasound
  • Intravascular optical coherence tomography is a catheter-based imaging modality that uses light to peer into coronary artery walls and generate images thereof for study. Utilizing coherent light, interferometry, and micro-optics, OCT can provide video-rate in-vivo tomography within a diseased vessel with micrometer level resolution. Viewing subsurface structures with high resolution using fiber-optic probes makes OCT especially useful for minimally invasive imaging of internal tissues and organs. This level of detail made possible with OCT allows a clinician to diagnose as well as monitor the progression of coronary artery disease.
  • Angiography is a noninvasive x-ray imaging method that collects data from outside the body during injection of a radio-opaque contrast fluid.
  • the disclosure relates to a multimodal diagnostic system and components thereof configured to co-register two or more of the following OCT, IVUS, FFR, and angiography.
  • OCT images and angiography images are co-registered after calibrating a combined OCT and x-ray imaging system to determine a time delay to align or synchronize the two sets of frames of image data.
  • the time delay is determined based upon a minimum value from multiple calibration trials.
  • angiography systems can be used to obtain a cine sequence or set of cine images. Such a set or sequence includes one or more images that are obtained over time. This set of images is effectively a short movie with each image being a frame that can track and show movement and cardiovascular system changes as the heart progresses through the cardiac cycle.
  • the initiation of an x-ray based imaging system such an angiography system can be caused by one or more control signals sent from one or more control systems.
  • the initiation of an intravascular imaging system such an OCT system can be caused by one or more control signals sent from one or more control systems to a patient interface unit or PIU.
  • the optical fiber and associated lens positioned to send and receive light rotates within a blood vessel.
  • the PIU to which an intravascular data collection probe connects receives a control signal which causes the probe tip to rotate and then translates the probe tip as part of a pullback through the blood vessel.
  • the probe tip captures an image along a ray or scan line as it rotates prior to translation along a support.
  • an angiography initiating control signal is transmitted prior to transmitting an OCT initiating control signal.
  • the angiography system captures one or more frames of angiography images such as J frames of angiography data prior to capturing a first frame of OCT image data.
  • the first frame of OCT image data can include images obtained while the probe tip rotates prior to being translated along a vessel during a pullback.
  • the disclosure relates to a method of calibrating a combination angiography and an optical coherence tomography (OCT) system.
  • the method can include acquiring angiography frames prior to initiation of an OCT probe pullback; acquiring OCT data during the OCT probe pullback; acquiring angiography frames during the OCT probe pullback; generating a plurality of OCT frames using the OCT data obtained during the pullback; determining an initial frame of the OCT probe pullback from the plurality of OCT frames; determining an initial angiography frame that corresponds to the initial frame of OCT probe pullback; determining a time delay between the initial OCT frame and the initial angiography frame; and aligning OCT and angiography frames using the time delay.
  • OCT optical coherence tomography
  • the method further includes displaying one or more aligned OCT frames and angiography frames.
  • determining a time delay includes performing a plurality of calibration trials to determine a plurality of delay periods and selecting the minimum delay period as the time delay.
  • the plurality of calibration trials is N trials, wherein N ranges from 2 trials to about 12 trials.
  • the method further includes initiating the OCT pullback at an initiation time, wherein a computing device stores the initiation time in memory.
  • determining the initial frame of the OCT probe pullback includes identifying the OCT frame corresponding to the initiation time as the initial frame of the OCT probe pullback.
  • determining the initial angiography frame includes determining a first angiography frame indicative of movement of a marker attached to the OCT probe and selecting a second angiography frame preceding the first angiography frame as the initial angiography frame.
  • the disclosure relates to a method of calibrating an optical coherence tomography system and an angiography system.
  • the method includes generating N sets of optical coherence tomography (OCT) image data, wherein each of the N sets of OCT image data is obtained by performing N ex vivo pullbacks of an intravascular data collection probe comprising a marker; generating N sets of angiography image data comprising a plurality of two-dimensional images, wherein each of the N sets of angiography image comprise a plurality of two-dimensional images of the marker in two or more different spatial positions; generating N sets of OCT frames using the N sets of OCT image data obtained during the N ex vivo pullbacks; determining an initial frame of the OCT probe pullback from the plurality of OCT frames for each set N; determining an initial angiography frame that corresponds to the initial frame of OCT probe pullback for each set N; determining a time delay between the initial OCT frame and the initial angiography frame for each set
  • determining the initial angiography frame includes determining a first angiography frame indicative of movement of a marker attached to the OCT probe and selecting a second angiography frame preceding the first angiography frame as the initial angiography frame.
  • N ranges from 2 to 12.
  • the method further includes initiating the OCT pullback at an initiation time, wherein a computing device stores the initiation time in memory.
  • determining the initial frame of the OCT probe pullback includes identifying the OCT frame corresponding to the initiation time as the initial frame of an ex vivo pullback.
  • determining the initial angiography frame includes using a computing device to track pixel changes in angiography frames to identify marker movement.
  • a frame rate of the OCT system is greater than the frame rate of the angiography system.
  • the disclosure relates to a system for calibrating a combination intravascular and extravascular imaging system.
  • the calibration system can include an x-ray based imaging subsystem and an optical imaging subsystem such as an interferometry-based subsystem.
  • the calibration system includes an optical coherence tomography (OCT) probe comprising a marker, wherein the probe is disposed on a support and disposed within an imaging zone of an angiography system; an optical coherence data processing system comprising a computing device, wherein the computing device generates frames of OCT images based upon received intravascular probe signals; one or more memory devices; and a control signal input in electrical communication with the one or more memory devices, wherein the control signal input is in electrical communication with a controller programmed to initiate a plurality of ex vivo pullbacks of the OCT probe and transmit each ex vivo pullback initiation time to the one or more memory devices.
  • OCT optical coherence tomography
  • the computing device can include, in an embodiment, a calibration method stored in the one or more memory device as instructions to cause the computing device to determine an initial frame of the OCT probe for each ex vivo pullback.
  • the computing device can include, in an embodiment, a calibration method stored in the one or more memory device as instructions to cause the computing device to determine an initial angiography frame that corresponds to the initial frame of OCT probe pullback.
  • the computing device can include, in an embodiment, a calibration method stored in the one or more memory device as instructions to cause the computing device to determine a time delay between the initial OCT frame and the initial angiography frame.
  • the computing device can include, in an embodiment, a calibration method stored in the one or more memory device as instructions to cause the computing device to align OCT and angiography frames using the time delay.
  • the disclosure relates to a method of imaging a blood vessel and/or calibrating a system that images a blood vessel.
  • the method includes generating a set of intravascular image data comprising a plurality of intravascular image frames at a first frame rate using an intravascular imaging system comprising a first clock; storing the intravascular image data in one or more non-transitory computer readable memory devices; generating a set of extravascular image data comprising a plurality of extravascular image frames at a second frame rate using an extravascular imaging system comprising a second clock; storing the extravascular image data in one or more non-transitory computer readable memory devices.
  • the method includes detecting motion in one of the plurality of frames. The frame preceding the frame having detected motion is selected as an initial frame in one embodiment.
  • the plurality of extravascular image frames comprises an angiography cine.
  • an intravascular data collection system collects data simultaneously with but asynchronously relative to an extravascular data collection system.
  • the method determines a delay or calibration period to synchronize frames obtained from the two asynchronous data collection systems.
  • the method can include co-registering the OCT image data and the angiography data by aligning one or more OCT frames with one or more angiography frames by a calibration time period.
  • the disclosure relates to a calibration method.
  • the method includes synchronizing x-ray image frames and intravascular image frames using a calibration period determined from a plurality of trials.
  • the method include programmatically generating a calibration period using an initial x-ray image frame having detected marker motion and an initial intravascular image frame determined by storing when a control signal to initiate marker motion is sent to an interface unit in mechanical communication with a marker and able to translate the marker over a plurality of positions.
  • the disclosure relates to a method of calibrating a combination angiography and an optical coherence tomography (OCT) system.
  • the method includes storing a plurality of angiography frames in one or more memory devices in electrical communication with a computing device; storing a plurality of OCT frames in one or more memory devices in electrical communication with the computing device, the OCT frames and angiography frames generated asynchronously during an overlapping time period corresponding to an OCT probe pullback; determining an initial frame of the OCT probe pullback from the plurality of OCT frames; determining an initial angiography frame that corresponds to the initial frame of OCT probe pullback; programmatically generating, using the computing device, a calibration period based upon a timestamp of the initial frame of OCT probe pullback and based upon a timestamp of the initial angiography frame; and synchronizing a plurality of the asynchronously generated OCT frames and angiography frames.
  • the computing device is a microprocessor or
  • FIG. 1 is a schematic diagram of a data collection system that collects intravascular data and extravascular data during overlapping periods of time suitable for calibration using one or more methods of the disclosure.
  • FIG. 2 is a schematic diagram of various data collection events and time periods that can be calibrated using one or more of the systems and methods described herein.
  • FIG. 3 is a schematic diagram illustrating various steps and events that can be implemented and tracked in conjunction with calibrating a multimodal imaging system and determining a calibration time period T 3 according to an embodiment of the disclosure.
  • FIG. 4 is a schematic diagram illustrating various steps of an exemplary temporal calibration method suitable for increasing co-registration accuracy in a multimodal imaging system according to an embodiment of the disclosure.
  • FIG. 5A is a schematic diagram of a data collection system that collects intravascular data and extravascular data during overlapping periods of time suitable for calibration using one or more methods of the disclosure.
  • FIG. 5B is a schematic diagram that depicts three x-ray image frames of a blood vessel being imaged using the system of FIG. 5A that correspond to three points in time when a marker is not moving and then movement starts and then movement continues during an OCT pullback of a probe according to an embodiment of the disclosure.
  • FIG. 6 illustrates an apparatus for performing temporal calibration according to an embodiment of the disclosure.
  • Intravascular data collection such as imaging of a blood vessel can be performed by inserting a catheter comprising a data collection probe into an artery and advancing it until it reaches a region of interest within a blood vessel, such a coronary artery.
  • An angiography system can obtain external angiographic images of that vessel, such as a cine sequence, during the imaging of the blood vessel.
  • the region of interest is imaged by pulling the data collection probe through the catheter while optical, acoustic, or other sensors in the probe collect intravascular data.
  • the process of pulling the data collecting probe through a region of interest in a blood vessel is referred to as a pullback in one embodiment. According to the disclosure, it is advantageous to initiate the angiography image capture prior to initiating the pullback for purposes of subsequently co-registering the angiographic and intravascular image data sets.
  • OCT/angiography or x-ray based coregistration facilitate visualization of a position of or a subset of an OCT image on a corresponding angiography image acquired at a similar point in time.
  • Such coregistration methods can be implemented using hardware, software, or combinations thereof
  • the disclosure relates to various systems, components thereof, and methods for use in a catheter lab or other facility to perform one or more calibration processes to improve co-registration accuracy with respect to data collected with regard to a subject.
  • the data can include one or more cine sequences obtained using an x-ray system such as an angiography system.
  • the data can include intravascular data.
  • An example of intravascular data is OCT data which can be obtained using an intravascular imaging probe and an OCT system.
  • the OCT data can be stored in computer-readable memory as scan lines, images, or in other data formats.
  • Intravascular ultrasound data is another type of intravascular data.
  • FIG. 1 shows a system 10 that includes various data collection subsystems suitable for collecting data, detecting a feature of, sensing a condition, and imaging a region of interest in a subject using one or more imaging modalities or otherwise generating diagnostic data.
  • the region of interest in a subject can include a blood vessel 15 .
  • an intravascular data collection probe is pulled back through the vessel 15 .
  • the probe includes one or more of a guidewire, a pressure sensing wire-based probe, an optical fiber and other components.
  • An optical fiber 18 is shown extending from where the probe would be disposed in the vessel 15 .
  • the tip of a given data collection probe can include a marker.
  • These markers are identified by M as shown herein in the non-invasively acquired image frames such as the x-ray generated images. As shown in FIG. 1 , a series of overlapping sequential angiography images are shown from a top down perspective with the dots corresponding to markers M shown over the sequence of their movement through the vessel 15 .
  • the marker M is a radiopaque marker that is part of the data collection probe.
  • a radiopaque marker M can be disposed near a lens or other beam-directing element of a probe.
  • the points F in the OCT frames are included to illustrate a feature F that changes its appearance as the pullback progresses. In this way, different cross-sections of the blood vessel being imaged with different features F correspond to different positions in the angiography frames.
  • the optical fiber is in optical communication with the beam director or lens.
  • a torque wire can be part of the probe defines a bore in which an optical fiber is disposed.
  • the probe also includes the sheath such as a polymer sheath (not shown) which forms part of a catheter.
  • the optical fiber which in the context of an OCT system is a portion of the sample arm of an interferometer, is optically coupled to a patient interface unit (PIU) as shown.
  • the PIU can be operated using various controls that can be used to initiate the pullback of the probe through the vessel.
  • the data collection system 10 includes a noninvasive imaging system 20 such as a nuclear magnetic resonance, x-ray, angiography, computer aided tomography, or other suitable noninvasive imaging technology.
  • a noninvasive imaging system 20 such as a nuclear magnetic resonance, x-ray, angiography, computer aided tomography, or other suitable noninvasive imaging technology.
  • an angiography system such as suitable for generating cines is shown.
  • the angiography system can include a fluoroscopy system.
  • the noninvasive imaging system collects extravascular or peripheral imaging data while the intravascular imaging probe pulled back through the vessel generates cross-sectional views 50 as shown. Theses intravascular images 50 can be cross-sectional view, longitudinal views, or other views generated using data from an intravascular data collection probe.
  • the noninvasive imaging system 20 and the PIU are in communication with separate data storage and processing systems 55 , 57 or can be in communication with one data storage and processing system 60 .
  • One or more of such systems 55 , 57 , or 60 can be used individually or integrated together.
  • These systems can be implemented as a workstation or server in one embodiment or generally as a computing device.
  • a computing device may include a server computer, a client user computer, a personal computer (PC), a laptop computer, a tablet PC, a desktop computer, a control system, a microprocessor or any computing device capable of executing a set of instructions (sequential or otherwise) that specify actions to be taken by that computing device.
  • the term “computing device” shall also be taken to include any collection of computing devices that individually or jointly execute a set (or multiple sets) of instructions to perform any one or more of the software features or methods such as interface.
  • the computing device is an optical coherence tomography computer programmed to perform one or more temporal calibration methods as described herein.
  • the programs, instructions, and control signal information and related co-registration methods that can use a calibration time can be implemented using software instructions stored in memory 65 or as a hardware-based integrated circuit 68 .
  • an external database 70 is used to store image frames, calibration time periods, co-registered OCT and x-ray images and other information described herein with respect to the systems and collected image data.
  • the time delay outputs of multiple calibration trials can be stored in memory such as database 70 or in the systems described herein and ranked to select a minimum time delay using one or more processors or computing devices.
  • memory 65 receives an OCT pullback initiation time corresponding to one the OCT probe pullback starts. This initiation time can be correlated with a corresponding captured OCT frame, which can be identified as the initial frame of the OCT pullback.
  • the patient interface unit includes a probe connector suitable to receive an end of the probe and be optically coupled thereto.
  • the PIU includes suitable joints and elements based on the type of data collection probe being used. In addition to being pulled back, the probe tip is also typically rotated by the PIU. In this way, a blood vessel of the subject 10 can be imaged longitudinally or via cross-sections.
  • the PIU is connected to one or more intravascular data collection systems 55 or 60 as described herein.
  • the intravascular data collection system 55 , 60 can be an OCT system, an IVUS system, another imaging system, and combinations of the foregoing.
  • the system 60 in the context of a probe being an OCT probe can include the sample arm of an interferometer, the reference arm of an interferometer, photodiodes, a control system, and patient interface unit.
  • the intravascular image data such as the frames of intravascular data generated using the data collection probe can be routed to the data collection processing system 60 coupled to the probe via PIU.
  • the noninvasive image data generated using system 20 can be transmitted to, stored in, and processed by one or more computing devices.
  • a video frame grabber device such as a computer board configured to capture the angiography image data from system 20 can be used in various embodiments as part of systems 55 , 57 , or 60 .
  • a set of angiography data such as cine sequence of images is acquired during an OCT pullback.
  • the marker M disposed on or in the OCT probe moves with it and is identifiable and trackable in the set of simultaneously captured angiography frames. If a coregistration calibration method of the angiography system and the OCT system is not performed or is inadequate to calibrate the relevant imaging system, the OCT frames and the angiography frames may not be aligned.
  • two steps are performed to achieve accurate coregistration in conjunction with a calibrated multimodal imaging system such as an OCT and angiography system.
  • the first step is identifying or locating a reference point or section of an intravascular data collection probe throughout a set of image frames such as angiography frames that constitute a cine sequence.
  • the reference point or section can include a marker, a probe tip, a lens, a pressure transducer, a beam director, or other probe locus, portion, component or combinations thereof. All of the foregoing can be used as markers M shown in the relevant figures.
  • a lens is used to direct and receive light and collect data that corresponds to depth measurements such that a tomographic image of the imaged region can be generated.
  • the second factor is temporally aligning the angiographic and OCT data sets.
  • the disclosure relates to calibration methods that can be performed when installing an OCT system in catheter lab to operate in conjunction with an angiography system.
  • the calibration of an OCT system is also performed when an angiography system is changed that is used in conjunction with the OCT system. When a change in such a multimodal imaging system occurs, re-calibration is often necessary to prevent or fix co-registration anomalies.
  • the calibration methods described herein improve the accuracy when co-registering a set of intravascular data, such as for example, a set of OCT images, and a set of peripheral or extravascular data such as a set of angiography images.
  • the disclosure relates to determining the relative time period between OCT and angiographic data sets. This time period can be determined and the can be used as a temporal calibration factor for the angiography coregistration software.
  • OCT and angiography image data are acquired simultaneously during an OCT catheter pullback with regard to blood vessel
  • a physical event E 1 in the real world (such as the initiation of the OCT catheter pullback) occurs at a certain point in time, indicated by the “Event” arrow such as a zero point in time, T 0 or some other origin or reference point.
  • This physical event E 1 is subsequently captured in an OCT image frame, which can be considered as a second event E 2 that is stored into computer memory at a future point in time “T 1 ” after the physical event.
  • the event capturing of the pullback initiation using OCT is event E 2 which corresponds to the imaging of the blood vessel 15 .
  • the angiography system lags the OCT system such that the angiography image capture of the blood vessel 15 and the moving OCT probe disposed therein is delayed by a delay period T 3 relative to the OCT image capture.
  • the same physical event E 1 is also captured in an angiography image frame that is stored into computer memory at a future point in time “T 2 ” after the physical event E 1 and after its OCT capture E 2 as effectively a third event E 3 .
  • the time periods T 1 and T 2 represent the finite time required to generate, transmit, and process the OCT and angiography images, respectively.
  • the time period T 1 ranges from about several microseconds to about several seconds.
  • the time period T 2 ranges from about several microseconds to about several seconds.
  • the time period T 3 ranges from about several microseconds to about several seconds.
  • the frame rate of an OCT system ranges from about 20 frames per second to about 1000 frames per second.
  • the frame rate of a non-invasive imaging system such as an x-ray-based system ranges from about 10 frames per second to about 60 frames per second.
  • T 1 and T 2 may be different, a fixed time period T 3 exists between when the OCT frame is stored into computer memory E 2 and when the corresponding angiography frame is stored into computer memory E 3 . If this time period T 3 is not compensated for, OCT frame positions are displayed on the incorrect angiography frame. In turn, such a failure to compensate for such a time lag T 3 can lead to inaccuracies in coregistration. As described herein, T 3 can be accurately determined using a calibration method.
  • the OCT and angiography data sets can be temporally aligned. After alignment using the determined T 3 value the OCT frame positions can be displayed on the correct angiography frame using the systems described herein.
  • One or more calibration systems 100 can be used to determine T 3 .
  • the calibration system can be implemented using one or more of the components of system 10 of FIG. 1 , system 110 of FIG. 5A and system 120 of FIG. 6 .
  • FIG. 3 illustrates a schematic representation of various image frames and method steps for determining the time period T 3 .
  • an OCT pullback is acquired with simultaneous angiography.
  • the frames shown at the top portion of FIG. 3 are frames of intravascular image data such as OCT data frames.
  • An OCT image feature F is visible at a position within each OCT data frame and changes position when the OCT pullback commences.
  • the frames below that include a top down view of an exemplary blood vessel are extravascular image data such as angiography data frames. Both datasets are generated, transmitted, processed, and stored in a central computer.
  • the OCT dataset includes frames of OCT image data numbered from 1 to 8. In contrast, three frames of angiography image data numbered 1 to 3 are also shown.
  • the OCT dataset includes a series of time stamped frames in the computer memory, where each timestamp represents the time at which the frame entered computer memory.
  • the corresponding series of time stamped angiography frames is also present in computer memory.
  • the timestamps are generated by a common system clock but are applied to each dataset independently.
  • the common system clock is the clock of the data processing system 60 .
  • the computer memory can be part of system 60 for example of FIG. 1 and similar data processing systems as described herein.
  • OCT frame represents the initial frame of the pullback.
  • a human may inspect the OCT image data and estimate which frame represents the initial frame of the pullback.
  • a computing device can be used to determine the initial frame of the pullback such as by automatically logging the time at which a command was sent to initiate the OCT pullback.
  • Machine vision and image processing software can also be used by a computing device to determine the initial frame of the pullback.
  • the initial OCT frame is the third frame of the dataset.
  • the initial angiography frame is the second frame of the dataset.
  • the radio-opaque marker M will not appear to move until the subsequent angio frame 3 , since the initial OCT pullback frame 3 is generated with the catheter at an initial resting position. Knowing the time stamps associated with OCT frame 3 and angiography frame 2 , the time period T 3 can be calculated and applied to realign the two datasets.
  • FIG. 4 includes an overview of these method steps and other related or supplemental steps as shown. Exemplary steps 10 to 80 are shown. Steps can be omitted as optional, performed simultaneously, or performed out of order in one or more embodiments.
  • the disclosure relates to the implementation of various steps or a subset thereof.
  • the steps include acquiring OCT data during OCT probe pullback; acquiring angiography data during OCT probe pullback; determining initial frame of OCT probe pullback from set of OCT frames; determining initial angiography frame that corresponds to initial frame of OCT probe pullback; determining time delay between initial OCT frame and initial angiography frame; selecting minimum time delay from multiple calibration trials; aligning OCT and angiography frames using minimum time delay; and displaying one or more aligned OCT and angiography frames.
  • FIG. 5A is a schematic diagram of an exemplary multimodal system that include an angiography system shown as non-invasive system 20 and an OCT system that includes a probe with a marker M that has been pulled back through the blood vessel 15 shown.
  • FIG. 5B shows the angiography frames corresponding to the pullback performed using the system of FIG. 5A .
  • a 1 At a time prior to the initiation of the pullback A 1 , there is no marker motion.
  • movement of the marker M occurs from rest moving from top to bottom from times A 1 to A 3 in the three angiography frames shown.
  • Angiography frame motion is detected using machine vision, human inspection, or another mechanism.
  • the angiography frame that is selected as the frame corresponding to initial probe or marker M movement is the frame before the frame for which motion is detected.
  • a 3 is not selected as the frame having initial movement. Instead, the frame before it, the middle frame corresponding to time A 2 is selected. If frame A 2 were detected as the frame having initial marker or probe motion then as part of the calibration method the first frame A 1 would be set as the initial movement angiography frame. This approach effectively sets the origin at which motion starts earlier to help improve calibration results.
  • frames of angiography data are processed, scanned or viewed to identify the occurrence of marker M movement or another probe feature. Once a frame has been identified as depicting probe movement, the frame immediately prior to that is identified for the purposes of the calibration method and the determination of time T 3 as the angiography frame having initial movement. This process of adjusting for movement errors has been found to improve system calibration by reducing the likelihood that the frame of initial movement is missed.
  • FIG. 6 illustrates a system 120 for conducting the temporal calibration methods described herein.
  • An imaging catheter 125 is placed on a support 130 within the field of view of the X-ray system 20 such as an angiography system.
  • the imaging catheter includes an intravascular imaging probe such as an OCT probe.
  • the OCT probe can be pulled back within a bore defined by the catheter.
  • the X-ray system 20 is activated first and acquires a cine sequence. If the OCT catheter includes a radio-opaque feature, such as a marker M, that moves in tandem with the catheter pullback, this motion will subsequently be visible on the acquired cine sequence.
  • a radio-opaque feature such as a marker M
  • a marker M disposed on the probe such as near the lens of the OCT probe translates within the bore of a catheter along the support 130 as one or more motors in the PIU pull a torque wire in which is disposed an optical fiber in optical communication with a lens or beam director.
  • Each frame of the angiography dataset is transmitted to an OCT computer, digitized by a frame grabber, and time stamped as the frame is stored in memory.
  • an OCT dataset is generated by an OCT engine and transmitted to the same OCT computing device.
  • Each OCT frame is time stamped as it enters memory.
  • the methods described herein such as shown in FIG. 2 can be executed and T 3 can be calculated.
  • the process of pulling an imaging probe back along a support while being imaged by an x-ray system can be performed a plurality of times to determine a set of candidate T 3 values for the intravascular and X-ray based systems.
  • selecting the appropriate T 3 value improves co-registration of frames generated by an intravascular system such as OCT and a non-invasive system such as angiography.
  • T 3 Angiography and angiography datasets are generated asynchronously (i.e., the OCT and angiography systems are independent devices with no master clocking mechanism).
  • the second source of T 3 errors or variation is that because the angiography frame rate is typically much lower than the OCT frame rate, the calculated value of T 3 may vary by up to +/ ⁇ one angiography frame period.
  • T 3 calibration delay period by repeated calculation and minimum value selection allows for an accurate assessment of the actual lag time period T 3 between the OCT and angiography datasets.
  • T 3 in an exemplary set of T 3 values can range from about 1 millisecond to about 500 milliseconds.
  • the smallest value in the set of N time delays is selected.
  • the smallest value has been determined to be a suitable estimate from N samples.
  • N ranges from 2 to 15.
  • N ranges from 4 to 10.
  • This error can be understood in terms of an angiography frame being shown as co-registered with a particular OCT or other intravascular imaging frame while the distance between wherein the respective frames are incorrectly aligned and as much as between greater than 0 mm to about 3 mm apart in terms of their actual respective location in a subject.
  • the present disclosure also relates to the apparatus for performing the operations herein.
  • This apparatus may be specially constructed for the required purposes, or it may comprise a general purpose computer selectively activated or reconfigured by a computer program stored in the computer.
  • Embodiments of the disclosure may be implemented in many different forms, including, but in no way limited to, computer program logic for use with a processor (e.g., a microprocessor, microcontroller, digital signal processor, or general purpose computer), programmable logic for use with a programmable logic device, (e.g., a Field Programmable Gate Array (FPGA) or other PLD), discrete components, integrated circuitry (e.g., an Application Specific Integrated Circuit (ASIC)), or any other means including any combination thereof.
  • a processor e.g., a microprocessor, microcontroller, digital signal processor, or general purpose computer
  • programmable logic for use with a programmable logic device e.g., a Field Programmable Gate Array (FPGA) or other PLD
  • FPGA Field Programmable Gate Array
  • ASIC Application Specific Integrated Circuit
  • some or all of the processing of the data collected using an OCT probe, an FFR probe, an angiography system, and other imaging and subject monitoring devices and the processor-based system is implemented as a set of computer program instructions that is converted into a computer executable form, stored as such in a computer readable medium, and executed by a microprocessor under the control of an operating system.
  • user interface instructions and triggers based upon the completion of a pullback or a co-registration request are transformed into processor understandable instructions suitable for generating OCT data, performing image procession using various and other features and embodiments described above.
  • Source code may include a series of computer program instructions implemented in any of various programming languages (e.g., an object code, an assembly language, or a high-level language such as Fortran, C, C++, JAVA, or HTML) for use with various operating systems or operating environments.
  • the source code may define and use various data structures and communication messages.
  • the source code may be in a computer executable form (e.g., via an interpreter), or the source code may be converted (e.g., via a translator, assembler, or compiler) into a computer executable form.
  • the computer program may be fixed in any form (e.g., source code form, computer executable form, or an intermediate form) either permanently or transitorily in a tangible storage medium, such as a semiconductor memory device (e.g., a RAM, ROM, PROM, EEPROM, or Flash-Programmable RAM), a magnetic memory device (e.g., a diskette or fixed disk), an optical memory device (e.g., a CD-ROM), a PC card (e.g., PCMCIA card), or other memory device.
  • a semiconductor memory device e.g., a RAM, ROM, PROM, EEPROM, or Flash-Programmable RAM
  • a magnetic memory device e.g., a diskette or fixed disk
  • an optical memory device e.g., a CD-ROM
  • PC card e.g., PCMCIA card
  • the computer program may be fixed in any form in a signal that is transmittable to a computer using any of various communication technologies, including, but in no way limited to, analog technologies, digital technologies, optical technologies, wireless technologies (e.g., Bluetooth), networking technologies, and internetworking technologies.
  • the computer program may be distributed in any form as a removable storage medium with accompanying printed or electronic documentation (e.g., shrink-wrapped software), preloaded with a computer system (e.g., on system ROM or fixed disk), or distributed from a server or electronic bulletin board over the communication system (e.g., the internet or World Wide Web).
  • Hardware logic including programmable logic for use with a programmable logic device
  • implementing all or part of the functionality previously described herein may be designed using traditional manual methods, or may be designed, captured, simulated, or documented electronically using various tools, such as Computer Aided Design (CAD), a hardware description language (e.g., VHDL or AHDL), or a PLD programming language (e.g., PALASM, ABEL, or CUPL).
  • CAD Computer Aided Design
  • a hardware description language e.g., VHDL or AHDL
  • PLD programming language e.g., PALASM, ABEL, or CUPL
  • Programmable logic may be fixed either permanently or transitorily in a tangible storage medium, such as a semiconductor memory device (e.g., a RAM, ROM, PROM, EEPROM, or Flash-Programmable RAM), a magnetic memory device (e.g., a diskette or fixed disk), an optical memory device (e.g., a CD-ROM), or other memory device.
  • a semiconductor memory device e.g., a RAM, ROM, PROM, EEPROM, or Flash-Programmable RAM
  • a magnetic memory device e.g., a diskette or fixed disk
  • an optical memory device e.g., a CD-ROM
  • the programmable logic may be fixed in a signal that is transmittable to a computer using any of various communication technologies, including, but in no way limited to, analog technologies, digital technologies, optical technologies, wireless technologies (e.g., Bluetooth), networking technologies, and internetworking technologies.
  • the programmable logic may be distributed as a removable storage medium with accompanying printed or electronic documentation (e.g., shrink-wrapped software), preloaded with a computer system (e.g., on system ROM or fixed disk), or distributed from a server or electronic bulletin board over the communication system (e.g., the internet or World Wide Web).
  • printed or electronic documentation e.g., shrink-wrapped software
  • a computer system e.g., on system ROM or fixed disk
  • server or electronic bulletin board e.g., the internet or World Wide Web
  • a module refers to software, hardware, or firmware suitable for performing a specific data processing or data transmission task.
  • a module refers to a software routine, program, or other memory resident application suitable for receiving, transforming, routing and processing instructions, or various types of data such as angiography data, OCT data, timestamps, calibration periods, marker position data, movement data, pixel information, calibration trial data and other information of interest as described herein.
  • Computers and computer systems described herein may include operatively associated computer-readable media such as memory for storing software applications used in obtaining, processing, storing and/or communicating data. It can be appreciated that such memory can be internal, external, remote or local with respect to its operatively associated computer or computer system.
  • Memory may also include any means for storing software or other instructions including, for example and without limitation, a hard disk, an optical disk, floppy disk, DVD (digital versatile disc), CD (compact disc), memory stick, flash memory, ROM (read only memory), RAM (random access memory), DRAM (dynamic random access memory), PROM (programmable ROM), EEPROM (extended erasable PROM), and/or other like computer-readable media.
  • a hard disk an optical disk, floppy disk, DVD (digital versatile disc), CD (compact disc), memory stick, flash memory, ROM (read only memory), RAM (random access memory), DRAM (dynamic random access memory), PROM (programmable ROM), EEPROM (extended erasable PROM), and/or other like computer-readable media.
  • computer-readable memory media applied in association with embodiments of the disclosure described herein may include any memory medium capable of storing instructions executed by a programmable apparatus. Where applicable, method steps described herein may be embodied or executed as instructions stored on a computer-readable memory medium or memory media. These instructions may be software embodied in various programming languages such as C++, C, Java, and/or a variety of other kinds of software programming languages that may be applied to create instructions in accordance with embodiments of the disclosure.
  • arrow heads showing directionality in a given figure or the lack thereof are not intended to limit or require a direction in which information can flow.
  • a given connector such as the arrows and lines shown connecting the elements shown in the figures information can flow in one or more directions or in only one direction as suitable for a given embodiment.
  • the connections can include various suitable data transmitting connections such as optical, wire, power, wireless, or electrical connections.
  • compositions are described as having, including, or comprising specific components, or where processes are described as having, including or comprising specific process steps, it is contemplated that compositions of the present teachings also consist essentially of, or consist of, the recited components, and that the processes of the present teachings also consist essentially of, or consist of, the recited process steps.
  • each intervening value between the upper and lower limits of that range or list of values is individually contemplated and is encompassed within the disclosure as if each value were specifically enumerated herein.
  • smaller ranges between and including the upper and lower limits of a given range are contemplated and encompassed within the disclosure.
  • the listing of exemplary values or ranges is not a disclaimer of other values or ranges between and including the upper and lower limits of a given range.

Abstract

In part, the disclosure relates to systems for imaging a blood vessel using intravascular image data and extravascular image data and methods to calibrate such systems. In one embodiment, multiple calibration trials are performed to determine a plurality of time lag values. A minimum time lag value is used to align intravascular image data and extravascular time lag data in one embodiment.

Description

FIELD
In part, the disclosure relates generally to the field of vascular system and peripheral vascular system imaging and data collection.
BACKGROUND
Interventional cardiologists incorporate a variety of diagnostic tools during catheterization procedures in order to plan, guide, and assess therapies. Fluoroscopy is generally used to perform angiographic imaging of blood vessels. In turn, such blood vessel imaging is used by physicians to diagnose, locate and treat blood vessel disease during interventions such as bypass surgery or stent placement. Intravascular imaging technologies such as optical coherence tomography (OCT) and acoustic technologies such as intravascular ultrasound (IVUS) and others are also valuable tools that can be used in lieu of or in combination with fluoroscopy to obtain high-resolution data regarding the condition of the blood vessels for a given subject.
Intravascular optical coherence tomography is a catheter-based imaging modality that uses light to peer into coronary artery walls and generate images thereof for study. Utilizing coherent light, interferometry, and micro-optics, OCT can provide video-rate in-vivo tomography within a diseased vessel with micrometer level resolution. Viewing subsurface structures with high resolution using fiber-optic probes makes OCT especially useful for minimally invasive imaging of internal tissues and organs. This level of detail made possible with OCT allows a clinician to diagnose as well as monitor the progression of coronary artery disease. Angiography is a noninvasive x-ray imaging method that collects data from outside the body during injection of a radio-opaque contrast fluid.
Given the complexity of the various technologies described above and the associated complexity of the datasets each of them generate, co-registering such datasets is difficult. If the relevant systems, such as for example an angiography system and an OCT system, are not calibrated to one another, the likelihood of achieving accurate co-registration is low.
Accordingly, a need therefore exists to provide suitable calibration methods and systems suitable for increasing coregistration accuracy. Embodiments of the disclosure address these challenges and others.
SUMMARY
In part, the disclosure relates to a multimodal diagnostic system and components thereof configured to co-register two or more of the following OCT, IVUS, FFR, and angiography. In one embodiment, OCT images and angiography images are co-registered after calibrating a combined OCT and x-ray imaging system to determine a time delay to align or synchronize the two sets of frames of image data. In one embodiment, the time delay is determined based upon a minimum value from multiple calibration trials. As discussed herein, angiography systems can be used to obtain a cine sequence or set of cine images. Such a set or sequence includes one or more images that are obtained over time. This set of images is effectively a short movie with each image being a frame that can track and show movement and cardiovascular system changes as the heart progresses through the cardiac cycle.
The initiation of an x-ray based imaging system such an angiography system can be caused by one or more control signals sent from one or more control systems. Similarly, the initiation of an intravascular imaging system such an OCT system can be caused by one or more control signals sent from one or more control systems to a patient interface unit or PIU. During an OCT data collection session, the optical fiber and associated lens positioned to send and receive light rotates within a blood vessel. The PIU to which an intravascular data collection probe connects receives a control signal which causes the probe tip to rotate and then translates the probe tip as part of a pullback through the blood vessel.
Initially, the probe tip captures an image along a ray or scan line as it rotates prior to translation along a support. In one embodiment, an angiography initiating control signal is transmitted prior to transmitting an OCT initiating control signal. As a result, the angiography system captures one or more frames of angiography images such as J frames of angiography data prior to capturing a first frame of OCT image data. The first frame of OCT image data can include images obtained while the probe tip rotates prior to being translated along a vessel during a pullback.
In part, the disclosure relates to a method of calibrating a combination angiography and an optical coherence tomography (OCT) system. The method can include acquiring angiography frames prior to initiation of an OCT probe pullback; acquiring OCT data during the OCT probe pullback; acquiring angiography frames during the OCT probe pullback; generating a plurality of OCT frames using the OCT data obtained during the pullback; determining an initial frame of the OCT probe pullback from the plurality of OCT frames; determining an initial angiography frame that corresponds to the initial frame of OCT probe pullback; determining a time delay between the initial OCT frame and the initial angiography frame; and aligning OCT and angiography frames using the time delay.
In one embodiment, the method further includes displaying one or more aligned OCT frames and angiography frames. In one embodiment, determining a time delay includes performing a plurality of calibration trials to determine a plurality of delay periods and selecting the minimum delay period as the time delay. In one embodiment, the plurality of calibration trials is N trials, wherein N ranges from 2 trials to about 12 trials. In one embodiment, the method further includes initiating the OCT pullback at an initiation time, wherein a computing device stores the initiation time in memory. In one embodiment, determining the initial frame of the OCT probe pullback includes identifying the OCT frame corresponding to the initiation time as the initial frame of the OCT probe pullback. In one embodiment, determining the initial angiography frame includes determining a first angiography frame indicative of movement of a marker attached to the OCT probe and selecting a second angiography frame preceding the first angiography frame as the initial angiography frame.
In part, in one embodiment, the disclosure relates to a method of calibrating an optical coherence tomography system and an angiography system. The method includes generating N sets of optical coherence tomography (OCT) image data, wherein each of the N sets of OCT image data is obtained by performing N ex vivo pullbacks of an intravascular data collection probe comprising a marker; generating N sets of angiography image data comprising a plurality of two-dimensional images, wherein each of the N sets of angiography image comprise a plurality of two-dimensional images of the marker in two or more different spatial positions; generating N sets of OCT frames using the N sets of OCT image data obtained during the N ex vivo pullbacks; determining an initial frame of the OCT probe pullback from the plurality of OCT frames for each set N; determining an initial angiography frame that corresponds to the initial frame of OCT probe pullback for each set N; determining a time delay between the initial OCT frame and the initial angiography frame for each set N such that N time delays are determined; selecting a minimum time delay from the N time delays; and aligning OCT and angiography frames using the minimum time delay.
In one embodiment of the method, determining the initial angiography frame includes determining a first angiography frame indicative of movement of a marker attached to the OCT probe and selecting a second angiography frame preceding the first angiography frame as the initial angiography frame. In one embodiment, N ranges from 2 to 12. In one embodiment, the method further includes initiating the OCT pullback at an initiation time, wherein a computing device stores the initiation time in memory. In one embodiment of the method, determining the initial frame of the OCT probe pullback includes identifying the OCT frame corresponding to the initiation time as the initial frame of an ex vivo pullback. In one embodiment, determining the initial angiography frame includes using a computing device to track pixel changes in angiography frames to identify marker movement. In one embodiment, a frame rate of the OCT system is greater than the frame rate of the angiography system.
In part, in one embodiment, the disclosure relates to a system for calibrating a combination intravascular and extravascular imaging system. The calibration system can include an x-ray based imaging subsystem and an optical imaging subsystem such as an interferometry-based subsystem. In one embodiment, the calibration system includes an optical coherence tomography (OCT) probe comprising a marker, wherein the probe is disposed on a support and disposed within an imaging zone of an angiography system; an optical coherence data processing system comprising a computing device, wherein the computing device generates frames of OCT images based upon received intravascular probe signals; one or more memory devices; and a control signal input in electrical communication with the one or more memory devices, wherein the control signal input is in electrical communication with a controller programmed to initiate a plurality of ex vivo pullbacks of the OCT probe and transmit each ex vivo pullback initiation time to the one or more memory devices.
The computing device can include, in an embodiment, a calibration method stored in the one or more memory device as instructions to cause the computing device to determine an initial frame of the OCT probe for each ex vivo pullback. The computing device can include, in an embodiment, a calibration method stored in the one or more memory device as instructions to cause the computing device to determine an initial angiography frame that corresponds to the initial frame of OCT probe pullback. The computing device can include, in an embodiment, a calibration method stored in the one or more memory device as instructions to cause the computing device to determine a time delay between the initial OCT frame and the initial angiography frame. The computing device can include, in an embodiment, a calibration method stored in the one or more memory device as instructions to cause the computing device to align OCT and angiography frames using the time delay.
In part, the disclosure relates to a method of imaging a blood vessel and/or calibrating a system that images a blood vessel. The method includes generating a set of intravascular image data comprising a plurality of intravascular image frames at a first frame rate using an intravascular imaging system comprising a first clock; storing the intravascular image data in one or more non-transitory computer readable memory devices; generating a set of extravascular image data comprising a plurality of extravascular image frames at a second frame rate using an extravascular imaging system comprising a second clock; storing the extravascular image data in one or more non-transitory computer readable memory devices. The method includes detecting motion in one of the plurality of frames. The frame preceding the frame having detected motion is selected as an initial frame in one embodiment. In one embodiment, the plurality of extravascular image frames comprises an angiography cine.
In one embodiment, an intravascular data collection system collects data simultaneously with but asynchronously relative to an extravascular data collection system. The method determines a delay or calibration period to synchronize frames obtained from the two asynchronous data collection systems. The method can include co-registering the OCT image data and the angiography data by aligning one or more OCT frames with one or more angiography frames by a calibration time period.
In one embodiment, the disclosure relates to a calibration method. The method includes synchronizing x-ray image frames and intravascular image frames using a calibration period determined from a plurality of trials. The method include programmatically generating a calibration period using an initial x-ray image frame having detected marker motion and an initial intravascular image frame determined by storing when a control signal to initiate marker motion is sent to an interface unit in mechanical communication with a marker and able to translate the marker over a plurality of positions.
In part, the disclosure relates to a method of calibrating a combination angiography and an optical coherence tomography (OCT) system. The method includes storing a plurality of angiography frames in one or more memory devices in electrical communication with a computing device; storing a plurality of OCT frames in one or more memory devices in electrical communication with the computing device, the OCT frames and angiography frames generated asynchronously during an overlapping time period corresponding to an OCT probe pullback; determining an initial frame of the OCT probe pullback from the plurality of OCT frames; determining an initial angiography frame that corresponds to the initial frame of OCT probe pullback; programmatically generating, using the computing device, a calibration period based upon a timestamp of the initial frame of OCT probe pullback and based upon a timestamp of the initial angiography frame; and synchronizing a plurality of the asynchronously generated OCT frames and angiography frames. In one embodiment, the computing device is a microprocessor or one or more circuits of an OCT data processing system. In one embodiment, the computing device is a microprocessor or one or more circuits of an angiography data processing system.
BRIEF DESCRIPTION OF THE DRAWINGS
The figures are not necessarily to scale, emphasis instead generally being placed upon illustrative principles. The figures are to be considered illustrative in all aspects and are not intended to limit the disclosure, the scope of which is defined only by the claims.
FIG. 1 is a schematic diagram of a data collection system that collects intravascular data and extravascular data during overlapping periods of time suitable for calibration using one or more methods of the disclosure.
FIG. 2 is a schematic diagram of various data collection events and time periods that can be calibrated using one or more of the systems and methods described herein.
FIG. 3 is a schematic diagram illustrating various steps and events that can be implemented and tracked in conjunction with calibrating a multimodal imaging system and determining a calibration time period T3 according to an embodiment of the disclosure.
FIG. 4 is a schematic diagram illustrating various steps of an exemplary temporal calibration method suitable for increasing co-registration accuracy in a multimodal imaging system according to an embodiment of the disclosure.
FIG. 5A is a schematic diagram of a data collection system that collects intravascular data and extravascular data during overlapping periods of time suitable for calibration using one or more methods of the disclosure.
FIG. 5B is a schematic diagram that depicts three x-ray image frames of a blood vessel being imaged using the system of FIG. 5A that correspond to three points in time when a marker is not moving and then movement starts and then movement continues during an OCT pullback of a probe according to an embodiment of the disclosure.
FIG. 6 illustrates an apparatus for performing temporal calibration according to an embodiment of the disclosure.
DETAILED DESCRIPTION
The following description refers to the accompanying drawings that illustrate certain embodiments of the present disclosure. Other embodiments are possible and modifications may be made to the embodiments without departing from the spirit and scope of the disclosure. Therefore, the following detailed description is not meant to limit the present disclosure; rather, the scope of the present disclosure is defined by the claims.
Intravascular data collection such as imaging of a blood vessel can be performed by inserting a catheter comprising a data collection probe into an artery and advancing it until it reaches a region of interest within a blood vessel, such a coronary artery. An angiography system can obtain external angiographic images of that vessel, such as a cine sequence, during the imaging of the blood vessel. In one embodiment, the region of interest is imaged by pulling the data collection probe through the catheter while optical, acoustic, or other sensors in the probe collect intravascular data. The process of pulling the data collecting probe through a region of interest in a blood vessel is referred to as a pullback in one embodiment. According to the disclosure, it is advantageous to initiate the angiography image capture prior to initiating the pullback for purposes of subsequently co-registering the angiographic and intravascular image data sets.
Co-registration of two or more imaging technologies such as angiography and OCT, for example, is challenging to implement. As disclosed herein, OCT/angiography or x-ray based coregistration (“angiography coregistration”) methods facilitate visualization of a position of or a subset of an OCT image on a corresponding angiography image acquired at a similar point in time. Such coregistration methods can be implemented using hardware, software, or combinations thereof
In part, the disclosure relates to various systems, components thereof, and methods for use in a catheter lab or other facility to perform one or more calibration processes to improve co-registration accuracy with respect to data collected with regard to a subject. In one embodiment, the data can include one or more cine sequences obtained using an x-ray system such as an angiography system. Further, the data can include intravascular data. An example of intravascular data is OCT data which can be obtained using an intravascular imaging probe and an OCT system. The OCT data can be stored in computer-readable memory as scan lines, images, or in other data formats. Intravascular ultrasound data is another type of intravascular data.
FIG. 1 shows a system 10 that includes various data collection subsystems suitable for collecting data, detecting a feature of, sensing a condition, and imaging a region of interest in a subject using one or more imaging modalities or otherwise generating diagnostic data. The region of interest in a subject can include a blood vessel 15. In one embodiment, an intravascular data collection probe is pulled back through the vessel 15.
Examples of such probes include OCT, IVUS, FRR, or other data collection probes. The probe includes one or more of a guidewire, a pressure sensing wire-based probe, an optical fiber and other components. An optical fiber 18 is shown extending from where the probe would be disposed in the vessel 15. The tip of a given data collection probe can include a marker. These markers are identified by M as shown herein in the non-invasively acquired image frames such as the x-ray generated images. As shown in FIG. 1, a series of overlapping sequential angiography images are shown from a top down perspective with the dots corresponding to markers M shown over the sequence of their movement through the vessel 15. In one embodiment, the marker M is a radiopaque marker that is part of the data collection probe. For example, in one embodiment, a radiopaque marker M can be disposed near a lens or other beam-directing element of a probe. The points F in the OCT frames are included to illustrate a feature F that changes its appearance as the pullback progresses. In this way, different cross-sections of the blood vessel being imaged with different features F correspond to different positions in the angiography frames.
For a probe that includes an optical beam director or lens, the optical fiber is in optical communication with the beam director or lens. A torque wire can be part of the probe defines a bore in which an optical fiber is disposed. In addition, the probe also includes the sheath such as a polymer sheath (not shown) which forms part of a catheter. The optical fiber, which in the context of an OCT system is a portion of the sample arm of an interferometer, is optically coupled to a patient interface unit (PIU) as shown. The PIU can be operated using various controls that can be used to initiate the pullback of the probe through the vessel.
The data collection system 10 includes a noninvasive imaging system 20 such as a nuclear magnetic resonance, x-ray, angiography, computer aided tomography, or other suitable noninvasive imaging technology. As shown as a non-limiting example of such a noninvasive imaging system, an angiography system such as suitable for generating cines is shown. The angiography system can include a fluoroscopy system. The noninvasive imaging system collects extravascular or peripheral imaging data while the intravascular imaging probe pulled back through the vessel generates cross-sectional views 50 as shown. Theses intravascular images 50 can be cross-sectional view, longitudinal views, or other views generated using data from an intravascular data collection probe.
The noninvasive imaging system 20 and the PIU are in communication with separate data storage and processing systems 55, 57 or can be in communication with one data storage and processing system 60. One or more of such systems 55, 57, or 60 can be used individually or integrated together. These systems can be implemented as a workstation or server in one embodiment or generally as a computing device. A computing device may include a server computer, a client user computer, a personal computer (PC), a laptop computer, a tablet PC, a desktop computer, a control system, a microprocessor or any computing device capable of executing a set of instructions (sequential or otherwise) that specify actions to be taken by that computing device. Further, while a single computing device is illustrated, the term “computing device” shall also be taken to include any collection of computing devices that individually or jointly execute a set (or multiple sets) of instructions to perform any one or more of the software features or methods such as interface.
In one embodiment, the computing device is an optical coherence tomography computer programmed to perform one or more temporal calibration methods as described herein. The programs, instructions, and control signal information and related co-registration methods that can use a calibration time can be implemented using software instructions stored in memory 65 or as a hardware-based integrated circuit 68. In one embodiment, an external database 70 is used to store image frames, calibration time periods, co-registered OCT and x-ray images and other information described herein with respect to the systems and collected image data. The time delay outputs of multiple calibration trials can be stored in memory such as database 70 or in the systems described herein and ranked to select a minimum time delay using one or more processors or computing devices. In one embodiment, memory 65 receives an OCT pullback initiation time corresponding to one the OCT probe pullback starts. This initiation time can be correlated with a corresponding captured OCT frame, which can be identified as the initial frame of the OCT pullback.
The patient interface unit includes a probe connector suitable to receive an end of the probe and be optically coupled thereto. The PIU includes suitable joints and elements based on the type of data collection probe being used. In addition to being pulled back, the probe tip is also typically rotated by the PIU. In this way, a blood vessel of the subject 10 can be imaged longitudinally or via cross-sections.
In turn, the PIU is connected to one or more intravascular data collection systems 55 or 60 as described herein. The intravascular data collection system 55, 60 can be an OCT system, an IVUS system, another imaging system, and combinations of the foregoing. For example, the system 60 in the context of a probe being an OCT probe can include the sample arm of an interferometer, the reference arm of an interferometer, photodiodes, a control system, and patient interface unit.
The intravascular image data such as the frames of intravascular data generated using the data collection probe can be routed to the data collection processing system 60 coupled to the probe via PIU. The noninvasive image data generated using system 20 can be transmitted to, stored in, and processed by one or more computing devices. A video frame grabber device such as a computer board configured to capture the angiography image data from system 20 can be used in various embodiments as part of systems 55, 57, or 60.
Calibration and Co-registration
In one embodiment of a coregistration method, a set of angiography data such a cine sequence of images is acquired during an OCT pullback. Thus, as an OCT imaging probe is pulled back through a blood vessel as it rotates, the marker M disposed on or in the OCT probe moves with it and is identifiable and trackable in the set of simultaneously captured angiography frames. If a coregistration calibration method of the angiography system and the OCT system is not performed or is inadequate to calibrate the relevant imaging system, the OCT frames and the angiography frames may not be aligned.
In turn, this results in a failure to coregister the x-ray and optical imaging datasets. In addition, the failure to align the OCT and angiography datasets could result in errors such as positional cursor errors. Thus, the cursor used by a clinician or other system operators used to show where the OCT image was taken on the angiography image may be out of sync by several frames. This can cause a lack confidence in system users such that they doubt that the on screen cursor is actually showing them what it purports to show them. Additional details relating to the problems of a time lag and misalignment of OCT image frames and angiography image frames is described in more detail with regards to FIG. 2 and calibration system 100.
In one embodiment, two steps are performed to achieve accurate coregistration in conjunction with a calibrated multimodal imaging system such as an OCT and angiography system. The first step is identifying or locating a reference point or section of an intravascular data collection probe throughout a set of image frames such as angiography frames that constitute a cine sequence. The reference point or section can include a marker, a probe tip, a lens, a pressure transducer, a beam director, or other probe locus, portion, component or combinations thereof. All of the foregoing can be used as markers M shown in the relevant figures.
Thus, for an OCT imaging probe, a lens is used to direct and receive light and collect data that corresponds to depth measurements such that a tomographic image of the imaged region can be generated. The second factor is temporally aligning the angiographic and OCT data sets. In part, the disclosure relates to calibration methods that can be performed when installing an OCT system in catheter lab to operate in conjunction with an angiography system. The calibration of an OCT system is also performed when an angiography system is changed that is used in conjunction with the OCT system. When a change in such a multimodal imaging system occurs, re-calibration is often necessary to prevent or fix co-registration anomalies.
The calibration methods described herein improve the accuracy when co-registering a set of intravascular data, such as for example, a set of OCT images, and a set of peripheral or extravascular data such as a set of angiography images. In part, the disclosure relates to determining the relative time period between OCT and angiographic data sets. This time period can be determined and the can be used as a temporal calibration factor for the angiography coregistration software.
As shown in FIG. 2, in an angiography coregistration system, OCT and angiography image data are acquired simultaneously during an OCT catheter pullback with regard to blood vessel A physical event E1 in the real world (such as the initiation of the OCT catheter pullback) occurs at a certain point in time, indicated by the “Event” arrow such as a zero point in time, T0 or some other origin or reference point. This physical event E1 is subsequently captured in an OCT image frame, which can be considered as a second event E2 that is stored into computer memory at a future point in time “T1” after the physical event. Thus, the event capturing of the pullback initiation using OCT is event E2 which corresponds to the imaging of the blood vessel 15. The angiography system lags the OCT system such that the angiography image capture of the blood vessel 15 and the moving OCT probe disposed therein is delayed by a delay period T3 relative to the OCT image capture.
Similarly, the same physical event E1 is also captured in an angiography image frame that is stored into computer memory at a future point in time “T2” after the physical event E1 and after its OCT capture E2 as effectively a third event E3. The time periods T1 and T2 represent the finite time required to generate, transmit, and process the OCT and angiography images, respectively. In one embodiment, the time period T1 ranges from about several microseconds to about several seconds. In one embodiment, the time period T2 ranges from about several microseconds to about several seconds. In one embodiment, the time period T3 ranges from about several microseconds to about several seconds. The frame rate of an OCT system ranges from about 20 frames per second to about 1000 frames per second. The frame rate of a non-invasive imaging system such as an x-ray-based system ranges from about 10 frames per second to about 60 frames per second.
Since T1 and T2 may be different, a fixed time period T3 exists between when the OCT frame is stored into computer memory E2 and when the corresponding angiography frame is stored into computer memory E3. If this time period T3 is not compensated for, OCT frame positions are displayed on the incorrect angiography frame. In turn, such a failure to compensate for such a time lag T3 can lead to inaccuracies in coregistration. As described herein, T3 can be accurately determined using a calibration method.
In turn, with a T3 value determined using the systems and methods described herein, the OCT and angiography data sets can be temporally aligned. After alignment using the determined T3 value the OCT frame positions can be displayed on the correct angiography frame using the systems described herein. One or more calibration systems 100 can be used to determine T3. The calibration system can be implemented using one or more of the components of system 10 of FIG. 1, system 110 of FIG. 5A and system 120 of FIG. 6.
FIG. 3 illustrates a schematic representation of various image frames and method steps for determining the time period T3. First, an OCT pullback is acquired with simultaneous angiography. The frames shown at the top portion of FIG. 3 are frames of intravascular image data such as OCT data frames. An OCT image feature F is visible at a position within each OCT data frame and changes position when the OCT pullback commences. The frames below that include a top down view of an exemplary blood vessel are extravascular image data such as angiography data frames. Both datasets are generated, transmitted, processed, and stored in a central computer. The OCT dataset includes frames of OCT image data numbered from 1 to 8. In contrast, three frames of angiography image data numbered 1 to 3 are also shown. The OCT dataset includes a series of time stamped frames in the computer memory, where each timestamp represents the time at which the frame entered computer memory. The corresponding series of time stamped angiography frames is also present in computer memory. The timestamps are generated by a common system clock but are applied to each dataset independently. In one embodiment, the common system clock is the clock of the data processing system 60. The computer memory can be part of system 60 for example of FIG. 1 and similar data processing systems as described herein.
Next, a determination is made as to which OCT frame represents the initial frame of the pullback. A human may inspect the OCT image data and estimate which frame represents the initial frame of the pullback. Alternatively, a computing device can be used to determine the initial frame of the pullback such as by automatically logging the time at which a command was sent to initiate the OCT pullback. Machine vision and image processing software can also be used by a computing device to determine the initial frame of the pullback. In the example shown in FIG. 3, the initial OCT frame is the third frame of the dataset.
Next, a determination is made as to which angiography frame represents the closest point in time to the initial OCT frame. This determination may also be made either by a human user or an automatic computer routine. Either a human user or a computer algorithm may inspect the angiography data and estimate which frame corresponds to the initial frame of the pullback. In the example shown in FIG. 3, the initial angiography frame is the second frame of the dataset. The radio-opaque marker M will not appear to move until the subsequent angio frame 3, since the initial OCT pullback frame 3 is generated with the catheter at an initial resting position. Knowing the time stamps associated with OCT frame 3 and angiography frame 2, the time period T3 can be calculated and applied to realign the two datasets. FIG. 4 includes an overview of these method steps and other related or supplemental steps as shown. Exemplary steps 10 to 80 are shown. Steps can be omitted as optional, performed simultaneously, or performed out of order in one or more embodiments.
In one embodiment, the disclosure relates to the implementation of various steps or a subset thereof. The steps include acquiring OCT data during OCT probe pullback; acquiring angiography data during OCT probe pullback; determining initial frame of OCT probe pullback from set of OCT frames; determining initial angiography frame that corresponds to initial frame of OCT probe pullback; determining time delay between initial OCT frame and initial angiography frame; selecting minimum time delay from multiple calibration trials; aligning OCT and angiography frames using minimum time delay; and displaying one or more aligned OCT and angiography frames.
FIG. 5A is a schematic diagram of an exemplary multimodal system that include an angiography system shown as non-invasive system 20 and an OCT system that includes a probe with a marker M that has been pulled back through the blood vessel 15 shown. FIG. 5B shows the angiography frames corresponding to the pullback performed using the system of FIG. 5A. At a time prior to the initiation of the pullback A1, there is no marker motion. As shown, movement of the marker M occurs from rest moving from top to bottom from times A1 to A3 in the three angiography frames shown. Angiography frame motion is detected using machine vision, human inspection, or another mechanism.
In one embodiment, the angiography frame that is selected as the frame corresponding to initial probe or marker M movement is the frame before the frame for which motion is detected. Thus, even if there is movement at time A2, if the first frame that is detected as having movement is at time A3, A3 is not selected as the frame having initial movement. Instead, the frame before it, the middle frame corresponding to time A2 is selected. If frame A2 were detected as the frame having initial marker or probe motion then as part of the calibration method the first frame A1 would be set as the initial movement angiography frame. This approach effectively sets the origin at which motion starts earlier to help improve calibration results.
In general, in one embodiment frames of angiography data are processed, scanned or viewed to identify the occurrence of marker M movement or another probe feature. Once a frame has been identified as depicting probe movement, the frame immediately prior to that is identified for the purposes of the calibration method and the determination of time T3 as the angiography frame having initial movement. This process of adjusting for movement errors has been found to improve system calibration by reducing the likelihood that the frame of initial movement is missed.
FIG. 6 illustrates a system 120 for conducting the temporal calibration methods described herein. The systems of FIGS. 1 and 5A and as otherwise described herein can also be used. An imaging catheter 125 is placed on a support 130 within the field of view of the X-ray system 20 such as an angiography system. In one embodiment, the imaging catheter includes an intravascular imaging probe such as an OCT probe. The OCT probe can be pulled back within a bore defined by the catheter. In one embodiment, the X-ray system 20 is activated first and acquires a cine sequence. If the OCT catheter includes a radio-opaque feature, such as a marker M, that moves in tandem with the catheter pullback, this motion will subsequently be visible on the acquired cine sequence.
In one embodiment, a marker M disposed on the probe such as near the lens of the OCT probe translates within the bore of a catheter along the support 130 as one or more motors in the PIU pull a torque wire in which is disposed an optical fiber in optical communication with a lens or beam director. Each frame of the angiography dataset is transmitted to an OCT computer, digitized by a frame grabber, and time stamped as the frame is stored in memory.
At the same time, an OCT dataset is generated by an OCT engine and transmitted to the same OCT computing device. Each OCT frame is time stamped as it enters memory. In this way the methods described herein such as shown in FIG. 2 can be executed and T3 can be calculated. The process of pulling an imaging probe back along a support while being imaged by an x-ray system can be performed a plurality of times to determine a set of candidate T3 values for the intravascular and X-ray based systems. As described herein, selecting the appropriate T3 value improves co-registration of frames generated by an intravascular system such as OCT and a non-invasive system such as angiography.
Based upon experimentation and testing to address errors detected during co-registration trials, it has been determined advantageous to conduct the temporal calibration procedure described above multiple times. By performing the calibration method multiple times it is possible to determine a more accurate assessment of T3. Performing multiple iterations of the calibration method to generate a set of T3 values addresses two sources of error. The first of these sources of T3 errors or variation is that OCT and angiography datasets are generated asynchronously (i.e., the OCT and angiography systems are independent devices with no master clocking mechanism). The second source of T3 errors or variation is that because the angiography frame rate is typically much lower than the OCT frame rate, the calculated value of T3 may vary by up to +/− one angiography frame period.
As a result of the lack of a master clocking system and the potential misalignment of frames due to frame rate differences, performing the calibration procedure multiple times and selecting the minimum value of T3 as a calibration parameter is performed. This optimization of the T3 calibration delay period by repeated calculation and minimum value selection allows for an accurate assessment of the actual lag time period T3 between the OCT and angiography datasets. Once a suitable T3 value has been determined, the OCT and angiography frames can be aligned on the same temporal reference frame. Each T3 in an exemplary set of T3 values can range from about 1 millisecond to about 500 milliseconds.
The smallest value in the set of N time delays is selected. The smallest value has been determined to be a suitable estimate from N samples. In one embodiment, N ranges from 2 to 15. In one embodiment, N ranges from 4 to 10. When a minimum T3 value from a set of N values is obtained, it can be used to identify an angiography frame, such as frame 2 in FIG. 3 which will have a relatively small amount of motion when compared for example to frame 3. The greater time lag associated with frame 3 results in the occurrence of a spatial positional error. This error can be understood in terms of an angiography frame being shown as co-registered with a particular OCT or other intravascular imaging frame while the distance between wherein the respective frames are incorrectly aligned and as much as between greater than 0 mm to about 3 mm apart in terms of their actual respective location in a subject.
Non-limiting Software Features and Embodiments for Implementing Angiography and Intravascular Data Calibration
The following description is intended to provide an overview of device hardware and other operating components suitable for performing the methods of the disclosure described herein. This description is not intended to limit the applicable environments or the scope of the disclosure. Similarly, the hardware and other operating components may be suitable as part of the apparatuses described above. The disclosure can be practiced with other system configurations, including personal computers, multiprocessor systems, microprocessor-based or programmable electronic devices, network PCs, minicomputers, mainframe computers, and the like.
Some portions of the detailed description are presented in terms of algorithms and symbolic representations of operations on data bits within a computer memory. These algorithmic descriptions and representations can be used by those skilled in the computer and software related fields. In one embodiment, an algorithm is here, and generally, conceived to be a self-consistent sequence of operations leading to a desired result. The operations performed as methods stops or otherwise described herein are those requiring physical manipulations of physical quantities. Usually, though not necessarily, these quantities take the form of electrical or magnetic signals capable of being stored, transferred, combined, transformed, compared, and otherwise manipulated.
Unless specifically stated otherwise as apparent from the following discussion, it is appreciated that throughout the description, discussions utilizing terms such as “processing” or “computing” or “calculating” or “comparing” or “aligning” or “synchronizing” or “operating” or “generating” or “co-registering” or “determining” or “displaying” or the like, refer to the action and processes of a computer system, or similar electronic computing device, that manipulates and transforms data represented as physical (electronic) quantities within the computer system's registers and memories into other data similarly represented as physical quantities within the computer system memories or registers or other such information storage, transmission or display devices.
The present disclosure, in some embodiments, also relates to the apparatus for performing the operations herein. This apparatus may be specially constructed for the required purposes, or it may comprise a general purpose computer selectively activated or reconfigured by a computer program stored in the computer.
The algorithms and displays presented herein are not inherently related to any particular computer or other apparatus. Various general purpose systems may be used with programs in accordance with the teachings herein, or it may prove convenient to construct more specialized apparatus to perform the required method steps. The required structure for a variety of these systems will appear from the description below.
Embodiments of the disclosure may be implemented in many different forms, including, but in no way limited to, computer program logic for use with a processor (e.g., a microprocessor, microcontroller, digital signal processor, or general purpose computer), programmable logic for use with a programmable logic device, (e.g., a Field Programmable Gate Array (FPGA) or other PLD), discrete components, integrated circuitry (e.g., an Application Specific Integrated Circuit (ASIC)), or any other means including any combination thereof. In a typical embodiment of the present disclosure, some or all of the processing of the data collected using an OCT probe, an FFR probe, an angiography system, and other imaging and subject monitoring devices and the processor-based system is implemented as a set of computer program instructions that is converted into a computer executable form, stored as such in a computer readable medium, and executed by a microprocessor under the control of an operating system. Thus, user interface instructions and triggers based upon the completion of a pullback or a co-registration request, for example, are transformed into processor understandable instructions suitable for generating OCT data, performing image procession using various and other features and embodiments described above.
Computer program logic implementing all or part of the functionality previously described herein may be embodied in various forms, including, but in no way limited to, a source code form, a computer executable form, and various intermediate forms (e.g., forms generated by an assembler, compiler, linker, or locator). Source code may include a series of computer program instructions implemented in any of various programming languages (e.g., an object code, an assembly language, or a high-level language such as Fortran, C, C++, JAVA, or HTML) for use with various operating systems or operating environments. The source code may define and use various data structures and communication messages. The source code may be in a computer executable form (e.g., via an interpreter), or the source code may be converted (e.g., via a translator, assembler, or compiler) into a computer executable form.
The computer program may be fixed in any form (e.g., source code form, computer executable form, or an intermediate form) either permanently or transitorily in a tangible storage medium, such as a semiconductor memory device (e.g., a RAM, ROM, PROM, EEPROM, or Flash-Programmable RAM), a magnetic memory device (e.g., a diskette or fixed disk), an optical memory device (e.g., a CD-ROM), a PC card (e.g., PCMCIA card), or other memory device. The computer program may be fixed in any form in a signal that is transmittable to a computer using any of various communication technologies, including, but in no way limited to, analog technologies, digital technologies, optical technologies, wireless technologies (e.g., Bluetooth), networking technologies, and internetworking technologies. The computer program may be distributed in any form as a removable storage medium with accompanying printed or electronic documentation (e.g., shrink-wrapped software), preloaded with a computer system (e.g., on system ROM or fixed disk), or distributed from a server or electronic bulletin board over the communication system (e.g., the internet or World Wide Web).
Hardware logic (including programmable logic for use with a programmable logic device) implementing all or part of the functionality previously described herein may be designed using traditional manual methods, or may be designed, captured, simulated, or documented electronically using various tools, such as Computer Aided Design (CAD), a hardware description language (e.g., VHDL or AHDL), or a PLD programming language (e.g., PALASM, ABEL, or CUPL).
Programmable logic may be fixed either permanently or transitorily in a tangible storage medium, such as a semiconductor memory device (e.g., a RAM, ROM, PROM, EEPROM, or Flash-Programmable RAM), a magnetic memory device (e.g., a diskette or fixed disk), an optical memory device (e.g., a CD-ROM), or other memory device. The programmable logic may be fixed in a signal that is transmittable to a computer using any of various communication technologies, including, but in no way limited to, analog technologies, digital technologies, optical technologies, wireless technologies (e.g., Bluetooth), networking technologies, and internetworking technologies. The programmable logic may be distributed as a removable storage medium with accompanying printed or electronic documentation (e.g., shrink-wrapped software), preloaded with a computer system (e.g., on system ROM or fixed disk), or distributed from a server or electronic bulletin board over the communication system (e.g., the internet or World Wide Web).
Various examples of suitable processing modules are discussed below in more detail. As used herein a module refers to software, hardware, or firmware suitable for performing a specific data processing or data transmission task. In one embodiment, a module refers to a software routine, program, or other memory resident application suitable for receiving, transforming, routing and processing instructions, or various types of data such as angiography data, OCT data, timestamps, calibration periods, marker position data, movement data, pixel information, calibration trial data and other information of interest as described herein.
Computers and computer systems described herein may include operatively associated computer-readable media such as memory for storing software applications used in obtaining, processing, storing and/or communicating data. It can be appreciated that such memory can be internal, external, remote or local with respect to its operatively associated computer or computer system.
Memory may also include any means for storing software or other instructions including, for example and without limitation, a hard disk, an optical disk, floppy disk, DVD (digital versatile disc), CD (compact disc), memory stick, flash memory, ROM (read only memory), RAM (random access memory), DRAM (dynamic random access memory), PROM (programmable ROM), EEPROM (extended erasable PROM), and/or other like computer-readable media.
In general, computer-readable memory media applied in association with embodiments of the disclosure described herein may include any memory medium capable of storing instructions executed by a programmable apparatus. Where applicable, method steps described herein may be embodied or executed as instructions stored on a computer-readable memory medium or memory media. These instructions may be software embodied in various programming languages such as C++, C, Java, and/or a variety of other kinds of software programming languages that may be applied to create instructions in accordance with embodiments of the disclosure.
The aspects, embodiments, features, and examples of the disclosure are to be considered illustrative in all respects and are not intended to limit the disclosure, the scope of which is defined only by the claims. Other embodiments, modifications, and usages will be apparent to those skilled in the art without departing from the spirit and scope of the claimed disclosure.
The use of headings and sections in the application is not meant to limit the disclosure; each section can apply to any aspect, embodiment, or feature of the disclosure.
The use of arrow heads showing directionality in a given figure or the lack thereof are not intended to limit or require a direction in which information can flow. For a given connector, such as the arrows and lines shown connecting the elements shown in the figures information can flow in one or more directions or in only one direction as suitable for a given embodiment. The connections can include various suitable data transmitting connections such as optical, wire, power, wireless, or electrical connections.
Throughout the application, where compositions are described as having, including, or comprising specific components, or where processes are described as having, including or comprising specific process steps, it is contemplated that compositions of the present teachings also consist essentially of, or consist of, the recited components, and that the processes of the present teachings also consist essentially of, or consist of, the recited process steps.
In the application, where an element or component is said to be included in and/or selected from a list of recited elements or components, it should be understood that the element or component can be any one of the recited elements or components and can be selected from a group consisting of two or more of the recited elements or components. Further, it should be understood that elements and/or features of a composition, an apparatus, or a method described herein can be combined in a variety of ways without departing from the spirit and scope of the present teachings, whether explicit or implicit herein.
The use of the terms “include,” “includes,” “including,” “have,” “has,” or “having” should be generally understood as open-ended and non-limiting unless specifically stated otherwise.
The use of the singular herein includes the plural (and vice versa) unless specifically stated otherwise. Moreover, the singular forms “a,” “an,” and “the” include plural forms unless the context clearly dictates otherwise. In addition, where the use of the term “about” is before a quantitative value, the present teachings also include the specific quantitative value itself, unless specifically stated otherwise.
It should be understood that the order of steps or order for performing certain actions is immaterial so long as the present teachings remain operable. Moreover, two or more steps or actions may be conducted simultaneously.
Where a range or list of values is provided, each intervening value between the upper and lower limits of that range or list of values is individually contemplated and is encompassed within the disclosure as if each value were specifically enumerated herein. In addition, smaller ranges between and including the upper and lower limits of a given range are contemplated and encompassed within the disclosure. The listing of exemplary values or ranges is not a disclaimer of other values or ranges between and including the upper and lower limits of a given range.
It should be appreciated that various aspects of the claimed disclosure are directed to subsets and substeps of the techniques disclosed herein. Further, the terms and expressions employed herein are used as terms of description and not of limitation, and there is no intention, in the use of such terms and expressions, of excluding any equivalents of the features shown and described or portions thereof, but it is recognized that various modifications are possible within the scope of the disclosure claimed. Accordingly, what is desired to be secured by Letters Patent is the disclosure as defined and differentiated in the following claims, including all equivalents.

Claims (12)

What is claimed is:
1. A calibration system comprising:
an optical coherence tomography (OCT) probe comprising a marker, wherein the probe is configured to collect OCT data, wherein the probe is disposed within an imaging zone of an angiography system;
an optical coherence tomography data processing system comprising
a computing device comprising a processor, the computing device programmed to generate frames of OCT images based upon received intravascular probe signals and to receive angiography data comprising angiography frames, the processor configured to cause the computing device to determine a minimum time delay between an initial OCT frame and an initial angiography frame from a set of time delays; and
one or more memory devices in electrical communication with the computing device; and
a controller programmed to initiate a plurality of pullbacks of the OCT probe, in response to a control signal, during which OCT data is collected, and transmit each pullback initiation time to the one or more memory devices.
2. The system of claim 1 wherein the computing device comprises a calibration method stored in the one or more memory devices as instructions to cause the computing device to determine an initial frame of the OCT probe for each pullback.
3. The system of claim 1 wherein the computing device comprises a calibration method stored in the one or more memory devices as instructions to cause the computing device to determine an initial angiography frame that corresponds to an initial frame of OCT probe pullback.
4. The system of claim 1 wherein the computing device comprises a calibration method stored in the one or more memory devices as instructions to cause the computing device to determine a time delay between an initial OCT frame and an initial angiography frame.
5. The system of claim 4 wherein the calibration method further comprises instructions to cause the computing device to align OCT frames and angiography frames using the time delay.
6. The system of claim 1 further comprising a display in electrical communication with the optical coherence data processing system, wherein the computing device is programmed to align one or more OCT frames and one or more angiography frames using the minimum time delay and display one or more of such aligned frames.
7. The system of claim 1 wherein a frame rate of the optical coherence tomography data processing system is greater than a frame rate of the angiography system.
8. The system of claim 1 wherein the computing device is programmed to track pixel changes in angiography frames to identify marker movement.
9. The system of claim 8 wherein the computing device is programmed to use to marker movement to determine an initial angiography frame.
10. The system of claim 8 wherein the computing device is programmed to align an OCT frame with an angiography frame in response to tracked marker positions.
11. The system of claim 1 wherein the computing device is programmed to store a time an OCT pullback is initiated in the one or more memory devices.
12. The system of claim 1 wherein the computing device is programmed to determine a time delay between an angiography frame and an OCT frame.
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PCT/US2015/042849 WO2016039884A1 (en) 2014-09-12 2015-07-30 Methods and system for temporal calibration of an intravascular imaging system
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20190154595A1 (en) * 2016-05-20 2019-05-23 Perimeter Medical Imaging, Inc. Method and system for combining microscopic imaging with x-ray
US11064873B2 (en) 2015-08-31 2021-07-20 Gentuity, Llc Imaging system includes imaging probe and delivery devices
US11278206B2 (en) 2015-04-16 2022-03-22 Gentuity, Llc Micro-optic probes for neurology
US11344373B2 (en) 2018-05-29 2022-05-31 Lightlab Imaging, Inc. Stent expansion display, systems, and methods
US11684242B2 (en) 2017-11-28 2023-06-27 Gentuity, Llc Imaging system

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10222956B2 (en) 2015-05-17 2019-03-05 Lightlab Imaging, Inc. Intravascular imaging user interface systems and methods
US10140712B2 (en) 2015-05-17 2018-11-27 Lightlab Imaging, Inc. Detection of stent struts relative to side branches
US9996921B2 (en) 2015-05-17 2018-06-12 LIGHTLAB IMAGING, lNC. Detection of metal stent struts
US10109058B2 (en) 2015-05-17 2018-10-23 Lightlab Imaging, Inc. Intravascular imaging system interfaces and stent detection methods
US10646198B2 (en) 2015-05-17 2020-05-12 Lightlab Imaging, Inc. Intravascular imaging and guide catheter detection methods and systems
EP3324830B1 (en) 2015-07-25 2023-01-04 Lightlab Imaging, Inc. Intravascular data visualization method and device
WO2017087477A1 (en) 2015-11-18 2017-05-26 Lightlab Imaging, Inc. Detection of stent struts relative to side branches
CN115998310A (en) 2015-11-23 2023-04-25 光学实验室成像公司 Detection and verification of shadows in intravascular images
JP7027331B2 (en) 2016-04-14 2022-03-01 ライトラボ・イメージング・インコーポレーテッド Identification of blood vessel branches
ES2854729T3 (en) 2016-05-16 2021-09-22 Lightlab Imaging Inc Method and system for the detection of self-expanding endoprosthesis, or stent, absorbable intravascular
WO2018017547A1 (en) * 2016-07-19 2018-01-25 Cygnus Investment Corporation C/O Solaris Corporate Services Ltd. Pressure sensing guidewire assemblies and systems
CN109716446B (en) 2016-09-28 2023-10-03 光学实验室成像公司 Stent planning system and method using vascular manifestations
EP3911239A4 (en) * 2019-03-08 2022-10-05 William E. Butler Temporal calibration of an angiographic imaging system
JP7426355B2 (en) * 2020-08-06 2024-02-01 キヤノン ユーエスエイ,インコーポレイテッド Automatic pullback trigger method for intracoronary imaging device or system with blood clearing
US20230389892A1 (en) * 2022-06-02 2023-12-07 Canon U.S.A., Inc. Devices, systems, and methods for automated delay detection between medical-imaging devices

Citations (159)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4548473A (en) 1983-05-12 1985-10-22 Honeywell Inc. Optical filter
JPS63127201A (en) 1986-11-17 1988-05-31 Matsushita Electric Ind Co Ltd Color filter
US5321501A (en) 1991-04-29 1994-06-14 Massachusetts Institute Of Technology Method and apparatus for optical imaging with means for controlling the longitudinal range of the sample
US5465147A (en) 1991-04-29 1995-11-07 Massachusetts Institute Of Technology Method and apparatus for acquiring images using a ccd detector array and no transverse scanner
US5509093A (en) 1993-10-13 1996-04-16 Micron Optics, Inc. Temperature compensated fiber fabry-perot filters
US5518810A (en) 1993-06-30 1996-05-21 Mitsubishi Materials Corporation Infrared ray cutoff material and infrared cutoff powder use for same
US5586201A (en) 1990-11-14 1996-12-17 Cedars-Sinai Medical Center Coronary tracking display
US5619368A (en) 1995-05-16 1997-04-08 Massachusetts Inst. Of Technology Optical frequency shifter
US5632767A (en) 1994-09-09 1997-05-27 Rare Earth Medical, Inc. Loop diffusers for diffusion of optical radiation
US5643253A (en) 1995-06-06 1997-07-01 Rare Earth Medical, Inc. Phototherapy apparatus with integral stopper device
US5715827A (en) 1994-09-02 1998-02-10 Cardiometrics, Inc. Ultra miniature pressure sensor and guide wire using the same and method
US5748598A (en) 1995-12-22 1998-05-05 Massachusetts Institute Of Technology Apparatus and methods for reading multilayer storage media using short coherence length sources
US5784352A (en) 1995-07-21 1998-07-21 Massachusetts Institute Of Technology Apparatus and method for accessing data on multilayered optical media
US5908415A (en) 1994-09-09 1999-06-01 Rare Earth Medical, Inc. Phototherapy methods and apparatus
US5947959A (en) 1994-09-09 1999-09-07 Rare Earth Medical, Inc. Phototherapeutic apparatus with diffusive tip assembly
US5965355A (en) 1995-09-21 1999-10-12 Agritope, Inc. Antibodies and proteins useful for assaying virus infection in grape plants
US6111645A (en) 1991-04-29 2000-08-29 Massachusetts Institute Of Technology Grating based phase control optical delay line
US6134003A (en) 1991-04-29 2000-10-17 Massachusetts Institute Of Technology Method and apparatus for performing optical measurements using a fiber optic imaging guidewire, catheter or endoscope
US6148095A (en) 1997-09-08 2000-11-14 University Of Iowa Research Foundation Apparatus and method for determining three-dimensional representations of tortuous vessels
US6160826A (en) 1991-04-29 2000-12-12 Massachusetts Institute Of Technology Method and apparatus for performing optical frequency domain reflectometry
US6191862B1 (en) 1999-01-20 2001-02-20 Lightlab Imaging, Llc Methods and apparatus for high speed longitudinal scanning in imaging systems
US6195445B1 (en) 1997-06-30 2001-02-27 Siemens Corporate Research, Inc. Motion compensation of an image sequence using optimal polyline tracking
US6270492B1 (en) 1994-09-09 2001-08-07 Cardiofocus, Inc. Phototherapeutic apparatus with diffusive tip assembly
US6302875B1 (en) 1996-10-11 2001-10-16 Transvascular, Inc. Catheters and related devices for forming passageways between blood vessels or other anatomical structures
US6348960B1 (en) 1998-11-06 2002-02-19 Kimotot Co., Ltd. Front scattering film
US6445939B1 (en) 1999-08-09 2002-09-03 Lightlab Imaging, Llc Ultra-small optical probes, imaging optics, and methods for using same
US20020161351A1 (en) 1998-09-01 2002-10-31 Samson Wilfred J. Method and apparatus for treating acute myocardial infarction with selective hypothermic perfusion
US6485413B1 (en) 1991-04-29 2002-11-26 The General Hospital Corporation Methods and apparatus for forward-directed optical scanning instruments
US6501551B1 (en) 1991-04-29 2002-12-31 Massachusetts Institute Of Technology Fiber optic imaging endoscope interferometer with at least one faraday rotator
US6552796B2 (en) 2001-04-06 2003-04-22 Lightlab Imaging, Llc Apparatus and method for selective data collection and signal to noise ratio enhancement using optical coherence tomography
US6564087B1 (en) 1991-04-29 2003-05-13 Massachusetts Institute Of Technology Fiber optic needle probes for optical coherence tomography imaging
US6565514B2 (en) 2000-08-25 2003-05-20 Radi Medical Systems Ab Method and system for determining physiological variables
US6570659B2 (en) 2001-03-16 2003-05-27 Lightlab Imaging, Llc Broadband light source system and method and light source combiner
US20040006277A1 (en) 2002-07-02 2004-01-08 Langenhove Glenn Van Determining vulnerable plaque in blood vessels
US6692824B2 (en) 1991-12-21 2004-02-17 Roehm Gmbh & Co. Kg Infrared-reflecting bodies
US6706004B2 (en) 2001-05-31 2004-03-16 Infraredx, Inc. Balloon catheter
US6718089B2 (en) 2001-02-16 2004-04-06 Indigo Medical Incorporated Optical fiber including a diffuser portion and continuous sleeve for the transmission of light
US6728566B1 (en) 2001-11-21 2004-04-27 Koninklijke Philips Electronics, N.V. Vessel tracking and tree extraction method and apparatus
US6731973B2 (en) 2001-06-12 2004-05-04 Ge Medical Systems Information Technologies, Inc. Method and apparatus for processing physiological data
US6760112B2 (en) 2001-02-17 2004-07-06 Lucent Technologies Inc. Grin-fiber lens based optical endoscopes
US20050043614A1 (en) 2003-08-21 2005-02-24 Huizenga Joel T. Automated methods and systems for vascular plaque detection and analysis
US6879851B2 (en) 2001-06-07 2005-04-12 Lightlab Imaging, Llc Fiber optic endoscopic gastrointestinal probe
US6891984B2 (en) 2002-07-25 2005-05-10 Lightlab Imaging, Llc Scanning miniature optical probes with optical distortion correction and rotational control
US6932809B2 (en) 2002-05-14 2005-08-23 Cardiofocus, Inc. Safety shut-off device for laser surgical instruments employing blackbody emitters
US6937696B1 (en) 1998-10-23 2005-08-30 Varian Medical Systems Technologies, Inc. Method and system for predictive physiological gating
US6942657B2 (en) 1999-07-14 2005-09-13 Cardiofocus, Inc. Intralumenal contact sensor
US6973202B2 (en) 1998-10-23 2005-12-06 Varian Medical Systems Technologies, Inc. Single-camera tracking of an object
US6974557B1 (en) 2001-12-18 2005-12-13 Advanced Cardiovasculer Systems, Inc. Methods for forming an optical window for an intracorporeal device and for joining parts
US20060095065A1 (en) 2004-09-24 2006-05-04 Tetsuaki Tanimura Fluid occluding devices and methods
US7068831B2 (en) 2000-08-31 2006-06-27 Koninklijke Philips Electronics, N.V. Image processing method and system for extracting a string of points following a threadlike structure in a sequence of images
US20060241465A1 (en) * 2005-01-11 2006-10-26 Volcano Corporation Vascular image co-registration
US7134994B2 (en) 2002-05-20 2006-11-14 Volcano Corporation Multipurpose host system for invasive cardiovascular diagnostic measurement acquisition and display
US20060264743A1 (en) 2005-05-06 2006-11-23 Siemens Aktiengesellschaft Method for tomographically displaying a cavity by optical coherence tomography (OCT) and an OCT device for carrying out the method
US20070024617A1 (en) 2005-08-01 2007-02-01 Ian Poole Method for determining a path along a biological object with a lumen
US20070027390A1 (en) 2005-07-13 2007-02-01 Michael Maschke System for performing and monitoring minimally invasive interventions
US7191100B2 (en) 1998-10-23 2007-03-13 Varian Medical Systems Technologies, Inc. Method and system for predictive physiological gating of radiation therapy
US20070066890A1 (en) 2005-09-22 2007-03-22 Siemens Aktiengesellschaft Catheter device
US7208333B2 (en) 2001-03-12 2007-04-24 Axsun Technologies, Inc. Process for fabricating MEMS membrane with integral mirror/lens
US7231243B2 (en) 2000-10-30 2007-06-12 The General Hospital Corporation Optical methods for tissue analysis
US20070135803A1 (en) 2005-09-14 2007-06-14 Amir Belson Methods and apparatus for performing transluminal and other procedures
US7241286B2 (en) 2003-04-25 2007-07-10 Lightlab Imaging, Llc Flush catheter with flow directing sheath
US7298478B2 (en) 2003-08-14 2007-11-20 Cytonome, Inc. Optical detector for a particle sorting system
US7301644B2 (en) 2004-12-02 2007-11-27 University Of Miami Enhanced optical coherence tomography for anatomical mapping
US7321677B2 (en) 2000-05-09 2008-01-22 Paieon Inc. System and method for three-dimensional reconstruction of an artery
US7412141B2 (en) 2004-11-16 2008-08-12 Biotex, Inc. Light diffusing tip
US20080194996A1 (en) * 2003-02-21 2008-08-14 Kassab Ghassan S Device, system and method for measuring cross-sectional areas in luminal organs
US7415049B2 (en) 2005-03-28 2008-08-19 Axsun Technologies, Inc. Laser with tilted multi spatial mode resonator tuning element
US7414779B2 (en) 2005-01-20 2008-08-19 Massachusetts Institute Of Technology Mode locking methods and apparatus
US20080221440A1 (en) 2007-03-08 2008-09-11 Sync-Rx, Ltd. Imaging and tools for use with moving organs
US20080283771A1 (en) * 2007-05-17 2008-11-20 General Electric Company System and method of combining ultrasound image acquisition with fluoroscopic image acquisition
USRE40608E1 (en) 1999-01-06 2008-12-16 Volcano Corporation Arrangement of IVUS system components including remote and adjacent components
US20090174931A1 (en) 2005-01-20 2009-07-09 Huber Robert A Fourier domain mode locking: method and apparatus for control and improved performance
US7593559B2 (en) 2005-11-18 2009-09-22 Duke University Method and system of coregistrating optical coherence tomography (OCT) with other clinical tests
US20090306520A1 (en) 2008-06-02 2009-12-10 Lightlab Imaging, Inc. Quantitative methods for obtaining tissue characteristics from optical coherence tomography images
US20100076320A1 (en) 2003-04-25 2010-03-25 Lightlab Imaging, Llc Flush catheter with flow directing sheath
US7697972B2 (en) 2002-11-19 2010-04-13 Medtronic Navigation, Inc. Navigation system for cardiac therapies
US7711413B2 (en) 2003-04-28 2010-05-04 Volcano Corporation Catheter imaging probe and method
US7729746B2 (en) 2005-11-04 2010-06-01 Siemens Aktiengesellschaft Three-dimensional co-registration between intravascular and angiographic data
US7742797B2 (en) 2005-06-30 2010-06-22 Siemens Aktiengesellschaft Device and method for intraluminal imaging for the reconstruction of 3D image data sets
US20100161022A1 (en) 2007-03-08 2010-06-24 Sync-Rx, Ltd. Pre-deployment positioning of an implantable device within a moving organ
JP2010148778A (en) 2008-12-26 2010-07-08 Toshiba Corp Image display and image display method
US7783337B2 (en) 2005-06-06 2010-08-24 Board Of Regents, The University Of Texas System OCT using spectrally resolved bandwidth
US7792342B2 (en) 2006-02-16 2010-09-07 Siemens Medical Solutions Usa, Inc. System and method for detecting and tracking a guidewire in a fluoroscopic image sequence
US7813609B2 (en) 2007-11-12 2010-10-12 Lightlab Imaging, Inc. Imaging catheter with integrated reference reflector
US7848791B2 (en) 2005-02-10 2010-12-07 Lightlab Imaging, Inc. Optical coherence tomography apparatus and methods
US7853316B2 (en) 2003-04-28 2010-12-14 Board Of Regents, The University Of Texas System Rotating optical catheter tip for optical coherence tomography
US7869663B2 (en) 2005-08-01 2011-01-11 Bioptigen, Inc. Methods, systems and computer program products for analyzing three dimensional data sets obtained from a sample
US7872759B2 (en) 2005-09-29 2011-01-18 The General Hospital Corporation Arrangements and methods for providing multimodality microscopic imaging of one or more biological structures
US20110071404A1 (en) 2009-09-23 2011-03-24 Lightlab Imaging, Inc. Lumen Morphology and Vascular Resistance Measurements Data Collection Systems, Apparatus and Methods
US7916387B2 (en) 2007-01-10 2011-03-29 Lightlab Imaging, Inc. Methods and apparatus for swept-source optical coherence tomography
US7918793B2 (en) 2005-10-28 2011-04-05 Biosense Webster, Inc. Synchronization of ultrasound imaging data with electrical mapping
US7925327B2 (en) 2002-12-04 2011-04-12 Koninklijke Philips Electronics N.V. Apparatus and method for assisting the navigation of a catheter in a vessel
US7935060B2 (en) 2006-11-08 2011-05-03 Lightlab Imaging, Inc. Opto-acoustic imaging devices and methods
US7967743B2 (en) 2006-02-23 2011-06-28 Olympus Corporation Endoscope observation device, observation device and observation method using endoscope
US20110157686A1 (en) 2008-09-03 2011-06-30 Lightlab Imaging, Inc. Wavelength-Tunable Light Source
US7991105B2 (en) 2006-10-17 2011-08-02 Koninklijke Philips Electronics N.V. Visualization of 3D images in combination with 2D projection images
US7988633B2 (en) 2005-10-12 2011-08-02 Volcano Corporation Apparatus and method for use of RFID catheter intelligence
US20110190586A1 (en) 2008-03-28 2011-08-04 Volcano Corporation Methods and systems for intravascular imaging and flushing
US20110228280A1 (en) 2010-03-17 2011-09-22 Lightlab Imaging, Inc. Intensity Noise Reduction Methods and Apparatus for Interferometric Sensing and Imaging Systems
US20110230758A1 (en) 2008-12-03 2011-09-22 Uzi Eichler System and method for determining the position of the tip of a medical catheter within the body of a patient
US8029447B2 (en) 2006-10-10 2011-10-04 Volcano Corporation Multipurpose host system for invasive cardiovascular diagnostic measurement acquisition including an enhanced dynamically configured graphical display
US20110319752A1 (en) * 2008-11-18 2011-12-29 Sync-Rx, Ltd. Image super enhancement
US20120004529A1 (en) 2007-03-08 2012-01-05 Sync-Rx, Ltd. Automatic display of previously-acquired endoluminal images
US20120004537A1 (en) 2007-03-08 2012-01-05 Sync-Rx, Ltd. Co-use of endoluminal data and extraluminal imaging
US20120029339A1 (en) * 2010-07-29 2012-02-02 Sync-Rx, Ltd. Accounting for forward motion during pullback of an endoluminal imaging probe
US20120075638A1 (en) 2010-08-02 2012-03-29 Case Western Reserve University Segmentation and quantification for intravascular optical coherence tomography images
US8206374B2 (en) 2010-03-15 2012-06-26 Medtronic Vascular, Inc. Catheter having improved traceability
US8206377B2 (en) 2009-12-22 2012-06-26 Lightlab Imaging, Inc. Torque limiter for an OCT catheter
US20120162660A1 (en) 2007-07-12 2012-06-28 Volcano Corporation Automatic calibration systems and methods of use
JP2012130680A (en) 2010-12-17 2012-07-12 General Electric Co <Ge> Synchronization for medical imaging systems
US8259303B2 (en) 2008-05-15 2012-09-04 Axsun Technologies, Inc. OCT combining probes and integrated systems
US20120224751A1 (en) 2007-07-12 2012-09-06 Volcano Corporation Automatic calibration systems and methods of use
US20120238869A1 (en) 2010-01-19 2012-09-20 Lightlab Imaging, Inc. Intravascular Optical Coherence Tomography System with Pressure Monitoring Interface and Accessories
US20120250028A1 (en) 2011-03-31 2012-10-04 Lightlab Imaging, Inc. Optical Buffering Methods, Apparatus, and Systems for Increasing the Repetition Rate of Tunable Light Sources
US8298147B2 (en) 2005-06-24 2012-10-30 Volcano Corporation Three dimensional co-registration for intravascular diagnosis and therapy
US20120310081A1 (en) 2011-05-31 2012-12-06 Lightlab Imaging, Inc. Multimodal Imaging System, Apparatus, and Methods
WO2012176191A1 (en) 2011-06-23 2012-12-27 Sync-Rx, Ltd. Luminal background cleaning
US20130006105A1 (en) 2011-06-30 2013-01-03 Terumo Kabushiki Kaisha Optical coherent tomographic image forming apparatus and control method thereof
US8351665B2 (en) 2005-04-28 2013-01-08 The General Hospital Corporation Systems, processes and software arrangements for evaluating information associated with an anatomical structure by an optical coherence ranging technique
US20130023761A1 (en) 2009-12-22 2013-01-24 Lightlab Imaging, Inc. Torque Limiter for an OCT Catheter
US20130051728A1 (en) 2011-08-31 2013-02-28 Lightlab Imaging, Inc. Optical Imaging Probes and Related Methods
US8412312B2 (en) 2009-09-23 2013-04-02 Lightlab Imaging, Inc. Apparatus, systems, and methods of in-vivo blood clearing in a lumen
US8423121B2 (en) 2008-08-11 2013-04-16 Siemens Aktiengesellschaft Method and system for guidewire tracking in fluoroscopic image sequences
US20130123616A1 (en) 2011-11-16 2013-05-16 Volcano Corporation Medical Workflow System and Method
US8457375B2 (en) 2009-09-25 2013-06-04 Siemens Aktiengesellschaft Visualization method and imaging system
US8457440B1 (en) 2009-01-27 2013-06-04 Axsun Technologies, Inc. Method and system for background subtraction in medical optical coherence tomography system
US8478387B2 (en) 2008-10-14 2013-07-02 Lightlab Imaging, Inc. Methods for stent strut detection and related measurement and display using optical coherence tomography
US20130281832A1 (en) 2012-04-24 2013-10-24 John Baumgart System for Coregistration of Optical Coherence Tomography and Angiographic X-ray Image Data
US8571639B2 (en) 2003-09-05 2013-10-29 Varian Medical Systems, Inc. Systems and methods for gating medical procedures
US8582109B1 (en) 2011-08-01 2013-11-12 Lightlab Imaging, Inc. Swept mode-hopping laser system, methods, and devices for frequency-domain optical coherence tomography
US8582619B2 (en) 2011-03-15 2013-11-12 Lightlab Imaging, Inc. Methods, systems, and devices for timing control in electromagnetic radiation sources
US8581643B1 (en) 2011-10-28 2013-11-12 Lightlab Imaging, Inc. Phase-lock loop-based clocking system, methods and apparatus
US8582934B2 (en) 2007-11-12 2013-11-12 Lightlab Imaging, Inc. Miniature optical elements for fiber-optic beam shaping
WO2013175472A2 (en) 2012-05-21 2013-11-28 Sync-Rx, Ltd. Co-use of endoluminal data and extraluminal imaging
WO2014002095A2 (en) 2012-06-26 2014-01-03 Sync-Rx, Ltd. Flow-related image processing in luminal organs
US20140024931A1 (en) 2012-07-20 2014-01-23 Lightlab Imaging, Inc. Data Encoders for Medical Devices and Related Methods
US8687201B2 (en) 2012-08-31 2014-04-01 Lightlab Imaging, Inc. Optical coherence tomography control systems and methods
US20140094691A1 (en) 2008-11-18 2014-04-03 Sync-Rx, Ltd. Apparatus and methods for mapping a sequence of images to a roadmap image
US20140094692A1 (en) 2008-11-18 2014-04-03 Sync-Rx, Ltd. Apparatus and methods for determining a dimension of a portion of a stack of endoluminal data points
US20140094697A1 (en) 2011-05-27 2014-04-03 Lightlab Imaging, Inc. Optical coherence tomography and pressure based systems and methods
US20140094689A1 (en) 2008-11-18 2014-04-03 Sync-Rx, Ltd. Apparatus and methods for determining a plurality of local calibration factors for an image
US20140094660A1 (en) * 2008-11-18 2014-04-03 Sync-Rx, Ltd. Accounting for non-uniform longitudinal motion during movement of an endoluminal imaging probe
US20140094693A1 (en) 2008-11-18 2014-04-03 Sync-Rx, Ltd. Accounting for skipped imaging locations during movement of an endoluminal imaging probe
US8700130B2 (en) 2007-03-08 2014-04-15 Sync-Rx, Ltd. Stepwise advancement of a medical tool
US20140142432A1 (en) 2012-11-19 2014-05-22 Christopher Hutchins Multimodal Imaging Systems, Probes and Methods
US20140142427A1 (en) 2012-11-16 2014-05-22 Lightlab Imaging, Inc. Automated Fluid Delivery Catheter and System
US20140187920A1 (en) 2012-12-31 2014-07-03 Volcano Corporation Devices, Systems, and Methods For Assessment of Vessels
US20140218210A1 (en) 2011-08-24 2014-08-07 Volcano Corporation Medical Communication Hub and Associated Methods
US8831321B1 (en) 2011-11-07 2014-09-09 Lightlab Imaging, Inc. Side branch detection methods, systems and devices
US20140270445A1 (en) 2013-03-13 2014-09-18 Volcano Corporation System and method for oct depth calibration
US20140268167A1 (en) 2013-03-15 2014-09-18 Lightlab Imaging, Inc. Calibration and Image Processing Devices, Methods, and Systems
US20140276011A1 (en) 2009-09-23 2014-09-18 Lightlab Imaging, Inc. Lumen Morphology and Vascular Resistance Measurements Data Collection Systems, Apparatus and Methods
US8855744B2 (en) 2008-11-18 2014-10-07 Sync-Rx, Ltd. Displaying a device within an endoluminal image stack
US20140309536A1 (en) 2011-06-30 2014-10-16 Lightlab Imaging, Inc. Catheter with flush valve and related systems and methods
US8909323B2 (en) 2009-08-06 2014-12-09 Siemens Medical Solutions Usa, Inc. System for processing angiography and ultrasound image data
US8913084B2 (en) 2012-12-21 2014-12-16 Volcano Corporation Method and apparatus for performing virtual pullback of an intravascular imaging device
US20140379269A1 (en) 2011-08-03 2014-12-25 Lightlab Imaging, Inc. Systems, methods and apparatus for determining a fractional flow reserve
US8953911B1 (en) 2011-10-28 2015-02-10 Lightlab Imaging, Inc. Spectroscopic imaging probes, devices, and methods
US20150141808A1 (en) * 2012-06-28 2015-05-21 Koninklijke Philips N.V. Fiber optic sensor guided navigation for vascular visualization and monitoring

Patent Citations (215)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4548473A (en) 1983-05-12 1985-10-22 Honeywell Inc. Optical filter
JPS63127201A (en) 1986-11-17 1988-05-31 Matsushita Electric Ind Co Ltd Color filter
US5586201A (en) 1990-11-14 1996-12-17 Cedars-Sinai Medical Center Coronary tracking display
US5822391A (en) 1990-11-14 1998-10-13 Cedar Sinai Medical Center Coronary tracking display
US6111645A (en) 1991-04-29 2000-08-29 Massachusetts Institute Of Technology Grating based phase control optical delay line
US5321501A (en) 1991-04-29 1994-06-14 Massachusetts Institute Of Technology Method and apparatus for optical imaging with means for controlling the longitudinal range of the sample
US6421164B2 (en) 1991-04-29 2002-07-16 Massachusetts Institute Of Technology Interferometeric imaging with a grating based phase control optical delay line
US5465147A (en) 1991-04-29 1995-11-07 Massachusetts Institute Of Technology Method and apparatus for acquiring images using a ccd detector array and no transverse scanner
US6485413B1 (en) 1991-04-29 2002-11-26 The General Hospital Corporation Methods and apparatus for forward-directed optical scanning instruments
US6282011B1 (en) 1991-04-29 2001-08-28 Massachusetts Institute Of Technology Grating based phase control optical delay line
US6501551B1 (en) 1991-04-29 2002-12-31 Massachusetts Institute Of Technology Fiber optic imaging endoscope interferometer with at least one faraday rotator
US6160826A (en) 1991-04-29 2000-12-12 Massachusetts Institute Of Technology Method and apparatus for performing optical frequency domain reflectometry
US5459570A (en) 1991-04-29 1995-10-17 Massachusetts Institute Of Technology Method and apparatus for performing optical measurements
US6564087B1 (en) 1991-04-29 2003-05-13 Massachusetts Institute Of Technology Fiber optic needle probes for optical coherence tomography imaging
US6134003A (en) 1991-04-29 2000-10-17 Massachusetts Institute Of Technology Method and apparatus for performing optical measurements using a fiber optic imaging guidewire, catheter or endoscope
US6692824B2 (en) 1991-12-21 2004-02-17 Roehm Gmbh & Co. Kg Infrared-reflecting bodies
US5518810A (en) 1993-06-30 1996-05-21 Mitsubishi Materials Corporation Infrared ray cutoff material and infrared cutoff powder use for same
US5509093A (en) 1993-10-13 1996-04-16 Micron Optics, Inc. Temperature compensated fiber fabry-perot filters
US5715827A (en) 1994-09-02 1998-02-10 Cardiometrics, Inc. Ultra miniature pressure sensor and guide wire using the same and method
US5908415A (en) 1994-09-09 1999-06-01 Rare Earth Medical, Inc. Phototherapy methods and apparatus
US5947959A (en) 1994-09-09 1999-09-07 Rare Earth Medical, Inc. Phototherapeutic apparatus with diffusive tip assembly
US6270492B1 (en) 1994-09-09 2001-08-07 Cardiofocus, Inc. Phototherapeutic apparatus with diffusive tip assembly
US5632767A (en) 1994-09-09 1997-05-27 Rare Earth Medical, Inc. Loop diffusers for diffusion of optical radiation
US5619368A (en) 1995-05-16 1997-04-08 Massachusetts Inst. Of Technology Optical frequency shifter
US5643253A (en) 1995-06-06 1997-07-01 Rare Earth Medical, Inc. Phototherapy apparatus with integral stopper device
US5784352A (en) 1995-07-21 1998-07-21 Massachusetts Institute Of Technology Apparatus and method for accessing data on multilayered optical media
US5965355A (en) 1995-09-21 1999-10-12 Agritope, Inc. Antibodies and proteins useful for assaying virus infection in grape plants
US5748598A (en) 1995-12-22 1998-05-05 Massachusetts Institute Of Technology Apparatus and methods for reading multilayer storage media using short coherence length sources
US6302875B1 (en) 1996-10-11 2001-10-16 Transvascular, Inc. Catheters and related devices for forming passageways between blood vessels or other anatomical structures
US6195445B1 (en) 1997-06-30 2001-02-27 Siemens Corporate Research, Inc. Motion compensation of an image sequence using optimal polyline tracking
US6148095A (en) 1997-09-08 2000-11-14 University Of Iowa Research Foundation Apparatus and method for determining three-dimensional representations of tortuous vessels
US20020161351A1 (en) 1998-09-01 2002-10-31 Samson Wilfred J. Method and apparatus for treating acute myocardial infarction with selective hypothermic perfusion
US6973202B2 (en) 1998-10-23 2005-12-06 Varian Medical Systems Technologies, Inc. Single-camera tracking of an object
US6937696B1 (en) 1998-10-23 2005-08-30 Varian Medical Systems Technologies, Inc. Method and system for predictive physiological gating
US7191100B2 (en) 1998-10-23 2007-03-13 Varian Medical Systems Technologies, Inc. Method and system for predictive physiological gating of radiation therapy
US6348960B1 (en) 1998-11-06 2002-02-19 Kimotot Co., Ltd. Front scattering film
USRE40608E1 (en) 1999-01-06 2008-12-16 Volcano Corporation Arrangement of IVUS system components including remote and adjacent components
US6191862B1 (en) 1999-01-20 2001-02-20 Lightlab Imaging, Llc Methods and apparatus for high speed longitudinal scanning in imaging systems
US6942657B2 (en) 1999-07-14 2005-09-13 Cardiofocus, Inc. Intralumenal contact sensor
US6445939B1 (en) 1999-08-09 2002-09-03 Lightlab Imaging, Llc Ultra-small optical probes, imaging optics, and methods for using same
US7321677B2 (en) 2000-05-09 2008-01-22 Paieon Inc. System and method for three-dimensional reconstruction of an artery
US6565514B2 (en) 2000-08-25 2003-05-20 Radi Medical Systems Ab Method and system for determining physiological variables
US7068831B2 (en) 2000-08-31 2006-06-27 Koninklijke Philips Electronics, N.V. Image processing method and system for extracting a string of points following a threadlike structure in a sequence of images
US7231243B2 (en) 2000-10-30 2007-06-12 The General Hospital Corporation Optical methods for tissue analysis
US6718089B2 (en) 2001-02-16 2004-04-06 Indigo Medical Incorporated Optical fiber including a diffuser portion and continuous sleeve for the transmission of light
US6760112B2 (en) 2001-02-17 2004-07-06 Lucent Technologies Inc. Grin-fiber lens based optical endoscopes
US7208333B2 (en) 2001-03-12 2007-04-24 Axsun Technologies, Inc. Process for fabricating MEMS membrane with integral mirror/lens
US6570659B2 (en) 2001-03-16 2003-05-27 Lightlab Imaging, Llc Broadband light source system and method and light source combiner
US6552796B2 (en) 2001-04-06 2003-04-22 Lightlab Imaging, Llc Apparatus and method for selective data collection and signal to noise ratio enhancement using optical coherence tomography
US6706004B2 (en) 2001-05-31 2004-03-16 Infraredx, Inc. Balloon catheter
US6879851B2 (en) 2001-06-07 2005-04-12 Lightlab Imaging, Llc Fiber optic endoscopic gastrointestinal probe
US6731973B2 (en) 2001-06-12 2004-05-04 Ge Medical Systems Information Technologies, Inc. Method and apparatus for processing physiological data
US6728566B1 (en) 2001-11-21 2004-04-27 Koninklijke Philips Electronics, N.V. Vessel tracking and tree extraction method and apparatus
US6974557B1 (en) 2001-12-18 2005-12-13 Advanced Cardiovasculer Systems, Inc. Methods for forming an optical window for an intracorporeal device and for joining parts
US6932809B2 (en) 2002-05-14 2005-08-23 Cardiofocus, Inc. Safety shut-off device for laser surgical instruments employing blackbody emitters
US8556820B2 (en) 2002-05-20 2013-10-15 Volcano Corporation Multipurpose host system for invasive cardiovascular diagnostic measurement acquisition and display
US7134994B2 (en) 2002-05-20 2006-11-14 Volcano Corporation Multipurpose host system for invasive cardiovascular diagnostic measurement acquisition and display
US8562537B2 (en) 2002-05-20 2013-10-22 Volcano Corporation Multipurpose host system for invasive cardiovascular diagnostic measurement acquisition and display
US20040006277A1 (en) 2002-07-02 2004-01-08 Langenhove Glenn Van Determining vulnerable plaque in blood vessels
US6891984B2 (en) 2002-07-25 2005-05-10 Lightlab Imaging, Llc Scanning miniature optical probes with optical distortion correction and rotational control
US20050201662A1 (en) 2002-07-25 2005-09-15 Petersen Christopher L. Scanning miniature optical probes with optical distortion correction and rotational control
US7697972B2 (en) 2002-11-19 2010-04-13 Medtronic Navigation, Inc. Navigation system for cardiac therapies
US7925327B2 (en) 2002-12-04 2011-04-12 Koninklijke Philips Electronics N.V. Apparatus and method for assisting the navigation of a catheter in a vessel
US20080194996A1 (en) * 2003-02-21 2008-08-14 Kassab Ghassan S Device, system and method for measuring cross-sectional areas in luminal organs
US20100076320A1 (en) 2003-04-25 2010-03-25 Lightlab Imaging, Llc Flush catheter with flow directing sheath
US7625366B2 (en) 2003-04-25 2009-12-01 Lightlab Imaging, Llc Flush catheter with flow directing sheath
US7241286B2 (en) 2003-04-25 2007-07-10 Lightlab Imaging, Llc Flush catheter with flow directing sheath
US7711413B2 (en) 2003-04-28 2010-05-04 Volcano Corporation Catheter imaging probe and method
US7853316B2 (en) 2003-04-28 2010-12-14 Board Of Regents, The University Of Texas System Rotating optical catheter tip for optical coherence tomography
US7298478B2 (en) 2003-08-14 2007-11-20 Cytonome, Inc. Optical detector for a particle sorting system
US7355699B2 (en) 2003-08-14 2008-04-08 Cytonome, Inc. Optical detector for a particle sorting system
US7576861B2 (en) 2003-08-14 2009-08-18 Cytonome/St, Llc Optical detector for a particle sorting system
US7492522B2 (en) 2003-08-14 2009-02-17 Cytonome, Inc. Optical detector for a particle sorting system
US20050043614A1 (en) 2003-08-21 2005-02-24 Huizenga Joel T. Automated methods and systems for vascular plaque detection and analysis
US8571639B2 (en) 2003-09-05 2013-10-29 Varian Medical Systems, Inc. Systems and methods for gating medical procedures
US20060095065A1 (en) 2004-09-24 2006-05-04 Tetsuaki Tanimura Fluid occluding devices and methods
US7412141B2 (en) 2004-11-16 2008-08-12 Biotex, Inc. Light diffusing tip
US7301644B2 (en) 2004-12-02 2007-11-27 University Of Miami Enhanced optical coherence tomography for anatomical mapping
US7930014B2 (en) 2005-01-11 2011-04-19 Volcano Corporation Vascular image co-registration
US20060241465A1 (en) * 2005-01-11 2006-10-26 Volcano Corporation Vascular image co-registration
US7414779B2 (en) 2005-01-20 2008-08-19 Massachusetts Institute Of Technology Mode locking methods and apparatus
US20090174931A1 (en) 2005-01-20 2009-07-09 Huber Robert A Fourier domain mode locking: method and apparatus for control and improved performance
US7848791B2 (en) 2005-02-10 2010-12-07 Lightlab Imaging, Inc. Optical coherence tomography apparatus and methods
US7415049B2 (en) 2005-03-28 2008-08-19 Axsun Technologies, Inc. Laser with tilted multi spatial mode resonator tuning element
US8351665B2 (en) 2005-04-28 2013-01-08 The General Hospital Corporation Systems, processes and software arrangements for evaluating information associated with an anatomical structure by an optical coherence ranging technique
US20060264743A1 (en) 2005-05-06 2006-11-23 Siemens Aktiengesellschaft Method for tomographically displaying a cavity by optical coherence tomography (OCT) and an OCT device for carrying out the method
US7408648B2 (en) 2005-05-06 2008-08-05 Siemens Aktiengesellschaft Method for tomographically displaying a cavity by optical coherence tomography (OCT) and an OCT device for carrying out the method
US7783337B2 (en) 2005-06-06 2010-08-24 Board Of Regents, The University Of Texas System OCT using spectrally resolved bandwidth
US8298147B2 (en) 2005-06-24 2012-10-30 Volcano Corporation Three dimensional co-registration for intravascular diagnosis and therapy
US7742797B2 (en) 2005-06-30 2010-06-22 Siemens Aktiengesellschaft Device and method for intraluminal imaging for the reconstruction of 3D image data sets
US20070027390A1 (en) 2005-07-13 2007-02-01 Michael Maschke System for performing and monitoring minimally invasive interventions
US7869663B2 (en) 2005-08-01 2011-01-11 Bioptigen, Inc. Methods, systems and computer program products for analyzing three dimensional data sets obtained from a sample
US20070024617A1 (en) 2005-08-01 2007-02-01 Ian Poole Method for determining a path along a biological object with a lumen
US20070135803A1 (en) 2005-09-14 2007-06-14 Amir Belson Methods and apparatus for performing transluminal and other procedures
US20070066890A1 (en) 2005-09-22 2007-03-22 Siemens Aktiengesellschaft Catheter device
US7872759B2 (en) 2005-09-29 2011-01-18 The General Hospital Corporation Arrangements and methods for providing multimodality microscopic imaging of one or more biological structures
US7988633B2 (en) 2005-10-12 2011-08-02 Volcano Corporation Apparatus and method for use of RFID catheter intelligence
US7918793B2 (en) 2005-10-28 2011-04-05 Biosense Webster, Inc. Synchronization of ultrasound imaging data with electrical mapping
US7729746B2 (en) 2005-11-04 2010-06-01 Siemens Aktiengesellschaft Three-dimensional co-registration between intravascular and angiographic data
US7593559B2 (en) 2005-11-18 2009-09-22 Duke University Method and system of coregistrating optical coherence tomography (OCT) with other clinical tests
US7792342B2 (en) 2006-02-16 2010-09-07 Siemens Medical Solutions Usa, Inc. System and method for detecting and tracking a guidewire in a fluoroscopic image sequence
US7967743B2 (en) 2006-02-23 2011-06-28 Olympus Corporation Endoscope observation device, observation device and observation method using endoscope
US8029447B2 (en) 2006-10-10 2011-10-04 Volcano Corporation Multipurpose host system for invasive cardiovascular diagnostic measurement acquisition including an enhanced dynamically configured graphical display
US7991105B2 (en) 2006-10-17 2011-08-02 Koninklijke Philips Electronics N.V. Visualization of 3D images in combination with 2D projection images
US7935060B2 (en) 2006-11-08 2011-05-03 Lightlab Imaging, Inc. Opto-acoustic imaging devices and methods
US20130012811A1 (en) 2006-11-08 2013-01-10 Lightlab Imaging, Inc. Opto-Acoustic Imaging Devices and Methods
US8449468B2 (en) 2006-11-08 2013-05-28 Lightlab Imaging, Inc. Opto-acoustic imaging devices and methods
US20140114182A1 (en) 2006-11-08 2014-04-24 Lightlab Imaging, Inc. Opto-Acoustic Imaging Devices and Methods
US20110101207A1 (en) 2007-01-10 2011-05-05 Lightlab Imaging, Inc. Methods and Apparatus for Swept-Source Optical Coherence Tomography
US8325419B2 (en) 2007-01-10 2012-12-04 Lightlab Imaging, Inc. Methods and apparatus for swept-source optical coherence tomography
US7916387B2 (en) 2007-01-10 2011-03-29 Lightlab Imaging, Inc. Methods and apparatus for swept-source optical coherence tomography
US20120004529A1 (en) 2007-03-08 2012-01-05 Sync-Rx, Ltd. Automatic display of previously-acquired endoluminal images
US20080221440A1 (en) 2007-03-08 2008-09-11 Sync-Rx, Ltd. Imaging and tools for use with moving organs
US20100172556A1 (en) 2007-03-08 2010-07-08 Sync-Rx, Ltd. Automatic enhancement of an image stream of a moving organ
US20100228076A1 (en) 2007-03-08 2010-09-09 Sync-Rx, Ltd Controlled actuation and deployment of a medical device
US20100191102A1 (en) 2007-03-08 2010-07-29 Sync-Rx, Ltd. Automatic correction and utilization of a vascular roadmap comprising a tool
US20100161023A1 (en) 2007-03-08 2010-06-24 Sync-Rx, Ltd. Automatic tracking of a tool upon a vascular roadmap
US8781193B2 (en) 2007-03-08 2014-07-15 Sync-Rx, Ltd. Automatic quantitative vessel analysis
US20100157041A1 (en) 2007-03-08 2010-06-24 Sync-Rx, Ltd. Automatic stabilization of an image stream of a moving organ
US20100160773A1 (en) 2007-03-08 2010-06-24 Sync-Rx, Ltd. Automatic quantitative vessel analysis at the location of an automatically-detected tool
US20100222671A1 (en) 2007-03-08 2010-09-02 Sync-Rx, Ltd. Identification and presentation of device-to-vessel relative motion
US8700130B2 (en) 2007-03-08 2014-04-15 Sync-Rx, Ltd. Stepwise advancement of a medical tool
US8693756B2 (en) 2007-03-08 2014-04-08 Sync-Rx, Ltd. Automatic reduction of interfering elements from an image stream of a moving organ
US20100160764A1 (en) 2007-03-08 2010-06-24 Sync-Rx, Ltd. Automatic generation and utilization of a vascular roadmap
US8670603B2 (en) 2007-03-08 2014-03-11 Sync-Rx, Ltd. Apparatus and methods for masking a portion of a moving image stream
US20100290693A1 (en) 2007-03-08 2010-11-18 Sync-Rx, Ltd. Location-sensitive cursor control and its use for vessel analysis
US20120004537A1 (en) 2007-03-08 2012-01-05 Sync-Rx, Ltd. Co-use of endoluminal data and extraluminal imaging
US20080221439A1 (en) 2007-03-08 2008-09-11 Sync-Rx, Ltd. Tools for use with moving organs
US8290228B2 (en) 2007-03-08 2012-10-16 Sync-Rx, Ltd. Location-sensitive cursor control and its use for vessel analysis
US20100161022A1 (en) 2007-03-08 2010-06-24 Sync-Rx, Ltd. Pre-deployment positioning of an implantable device within a moving organ
US8463007B2 (en) 2007-03-08 2013-06-11 Sync-Rx, Ltd. Automatic generation of a vascular skeleton
US20080221442A1 (en) 2007-03-08 2008-09-11 Sync-Rx, Ltd. Imaging for use with moving organs
US8542900B2 (en) 2007-03-08 2013-09-24 Sync-Rx Ltd. Automatic reduction of interfering elements from an image stream of a moving organ
US20080283771A1 (en) * 2007-05-17 2008-11-20 General Electric Company System and method of combining ultrasound image acquisition with fluoroscopic image acquisition
US20120162660A1 (en) 2007-07-12 2012-06-28 Volcano Corporation Automatic calibration systems and methods of use
US20120224751A1 (en) 2007-07-12 2012-09-06 Volcano Corporation Automatic calibration systems and methods of use
US8582934B2 (en) 2007-11-12 2013-11-12 Lightlab Imaging, Inc. Miniature optical elements for fiber-optic beam shaping
US20140249407A1 (en) 2007-11-12 2014-09-04 Lightlab Imaging, Inc. Miniature Optical Elements for Fiber-Optic Beam Shaping
US8116605B2 (en) 2007-11-12 2012-02-14 Lightlab Imaging, Inc. Imaging catheter with integrated reference reflector
US8503844B2 (en) 2007-11-12 2013-08-06 Lightlab Imaging, Inc. Imaging catheter with integrated reference reflector
US20130010303A1 (en) 2007-11-12 2013-01-10 Lightlab Imaging, Inc. Imaging Catheter With Integrated Reference Reflector
US7813609B2 (en) 2007-11-12 2010-10-12 Lightlab Imaging, Inc. Imaging catheter with integrated reference reflector
US20110190586A1 (en) 2008-03-28 2011-08-04 Volcano Corporation Methods and systems for intravascular imaging and flushing
US20120300216A1 (en) 2008-05-15 2012-11-29 Axsun Technologies, Inc. Integrated Optical Coherence Analysis System
US20120300215A1 (en) 2008-05-15 2012-11-29 Axsun Technologies, Inc. OCT Combining Probes and Integrated Systems
US8259303B2 (en) 2008-05-15 2012-09-04 Axsun Technologies, Inc. OCT combining probes and integrated systems
US20090306520A1 (en) 2008-06-02 2009-12-10 Lightlab Imaging, Inc. Quantitative methods for obtaining tissue characteristics from optical coherence tomography images
US8423121B2 (en) 2008-08-11 2013-04-16 Siemens Aktiengesellschaft Method and system for guidewire tracking in fluoroscopic image sequences
US8358461B2 (en) 2008-09-03 2013-01-22 Lightlab Imaging Inc. Wavelength-tunable light source
US20110157686A1 (en) 2008-09-03 2011-06-30 Lightlab Imaging, Inc. Wavelength-Tunable Light Source
US20140018669A1 (en) 2008-10-14 2014-01-16 Lightlab Imaging, Inc. Methods for Stent Strut Detection and Related Measurement and Display Using Optical Coherence Tomography
US8478387B2 (en) 2008-10-14 2013-07-02 Lightlab Imaging, Inc. Methods for stent strut detection and related measurement and display using optical coherence tomography
US20140094660A1 (en) * 2008-11-18 2014-04-03 Sync-Rx, Ltd. Accounting for non-uniform longitudinal motion during movement of an endoluminal imaging probe
US8855744B2 (en) 2008-11-18 2014-10-07 Sync-Rx, Ltd. Displaying a device within an endoluminal image stack
US20140094692A1 (en) 2008-11-18 2014-04-03 Sync-Rx, Ltd. Apparatus and methods for determining a dimension of a portion of a stack of endoluminal data points
US20140094691A1 (en) 2008-11-18 2014-04-03 Sync-Rx, Ltd. Apparatus and methods for mapping a sequence of images to a roadmap image
US20140094689A1 (en) 2008-11-18 2014-04-03 Sync-Rx, Ltd. Apparatus and methods for determining a plurality of local calibration factors for an image
US20110319752A1 (en) * 2008-11-18 2011-12-29 Sync-Rx, Ltd. Image super enhancement
US20140094693A1 (en) 2008-11-18 2014-04-03 Sync-Rx, Ltd. Accounting for skipped imaging locations during movement of an endoluminal imaging probe
US20110230758A1 (en) 2008-12-03 2011-09-22 Uzi Eichler System and method for determining the position of the tip of a medical catheter within the body of a patient
JP2010148778A (en) 2008-12-26 2010-07-08 Toshiba Corp Image display and image display method
US8457440B1 (en) 2009-01-27 2013-06-04 Axsun Technologies, Inc. Method and system for background subtraction in medical optical coherence tomography system
US8909323B2 (en) 2009-08-06 2014-12-09 Siemens Medical Solutions Usa, Inc. System for processing angiography and ultrasound image data
US20130072805A1 (en) 2009-09-23 2013-03-21 Lightlab Imaging, Inc. Lumen Morphology and Vascular Resistance Measurements Data Collection Systems, Apparatus and Methods
US20110071404A1 (en) 2009-09-23 2011-03-24 Lightlab Imaging, Inc. Lumen Morphology and Vascular Resistance Measurements Data Collection Systems, Apparatus and Methods
US20130310698A1 (en) 2009-09-23 2013-11-21 Lightlab Imaging, Inc. Apparatus, Systems, and Methods of In-Vivo Blood Clearing in a Lumen
US8412312B2 (en) 2009-09-23 2013-04-02 Lightlab Imaging, Inc. Apparatus, systems, and methods of in-vivo blood clearing in a lumen
US20140276011A1 (en) 2009-09-23 2014-09-18 Lightlab Imaging, Inc. Lumen Morphology and Vascular Resistance Measurements Data Collection Systems, Apparatus and Methods
US8457375B2 (en) 2009-09-25 2013-06-04 Siemens Aktiengesellschaft Visualization method and imaging system
US8206377B2 (en) 2009-12-22 2012-06-26 Lightlab Imaging, Inc. Torque limiter for an OCT catheter
US20130023761A1 (en) 2009-12-22 2013-01-24 Lightlab Imaging, Inc. Torque Limiter for an OCT Catheter
US20140187929A1 (en) 2010-01-19 2014-07-03 Lightlab Imaging, Inc. Intravascular Optical Coherence Tomography System with Pressure Monitoring Interface and Accessories
US8478384B2 (en) 2010-01-19 2013-07-02 Lightlab Imaging, Inc. Intravascular optical coherence tomography system with pressure monitoring interface and accessories
US20120238869A1 (en) 2010-01-19 2012-09-20 Lightlab Imaging, Inc. Intravascular Optical Coherence Tomography System with Pressure Monitoring Interface and Accessories
US8206374B2 (en) 2010-03-15 2012-06-26 Medtronic Vascular, Inc. Catheter having improved traceability
US20110228280A1 (en) 2010-03-17 2011-09-22 Lightlab Imaging, Inc. Intensity Noise Reduction Methods and Apparatus for Interferometric Sensing and Imaging Systems
JP2013537444A (en) 2010-07-29 2013-10-03 エスワイエヌシー−アールエックス、リミテッド Combined use of intraluminal data and extraluminal imaging
US20120029339A1 (en) * 2010-07-29 2012-02-02 Sync-Rx, Ltd. Accounting for forward motion during pullback of an endoluminal imaging probe
US20120075638A1 (en) 2010-08-02 2012-03-29 Case Western Reserve University Segmentation and quantification for intravascular optical coherence tomography images
JP2012130680A (en) 2010-12-17 2012-07-12 General Electric Co <Ge> Synchronization for medical imaging systems
US8948228B2 (en) 2011-03-15 2015-02-03 Lightlab Imaging, Inc. Methods, systems, and devices for timing control in electromagnetic radiation sources
US8582619B2 (en) 2011-03-15 2013-11-12 Lightlab Imaging, Inc. Methods, systems, and devices for timing control in electromagnetic radiation sources
US20120250028A1 (en) 2011-03-31 2012-10-04 Lightlab Imaging, Inc. Optical Buffering Methods, Apparatus, and Systems for Increasing the Repetition Rate of Tunable Light Sources
US20140094697A1 (en) 2011-05-27 2014-04-03 Lightlab Imaging, Inc. Optical coherence tomography and pressure based systems and methods
US20120310081A1 (en) 2011-05-31 2012-12-06 Lightlab Imaging, Inc. Multimodal Imaging System, Apparatus, and Methods
WO2012176191A1 (en) 2011-06-23 2012-12-27 Sync-Rx, Ltd. Luminal background cleaning
US20130006105A1 (en) 2011-06-30 2013-01-03 Terumo Kabushiki Kaisha Optical coherent tomographic image forming apparatus and control method thereof
US20140309536A1 (en) 2011-06-30 2014-10-16 Lightlab Imaging, Inc. Catheter with flush valve and related systems and methods
US8582109B1 (en) 2011-08-01 2013-11-12 Lightlab Imaging, Inc. Swept mode-hopping laser system, methods, and devices for frequency-domain optical coherence tomography
US20140379269A1 (en) 2011-08-03 2014-12-25 Lightlab Imaging, Inc. Systems, methods and apparatus for determining a fractional flow reserve
US20140218210A1 (en) 2011-08-24 2014-08-07 Volcano Corporation Medical Communication Hub and Associated Methods
US20130051728A1 (en) 2011-08-31 2013-02-28 Lightlab Imaging, Inc. Optical Imaging Probes and Related Methods
US8953911B1 (en) 2011-10-28 2015-02-10 Lightlab Imaging, Inc. Spectroscopic imaging probes, devices, and methods
US8581643B1 (en) 2011-10-28 2013-11-12 Lightlab Imaging, Inc. Phase-lock loop-based clocking system, methods and apparatus
US8786336B1 (en) 2011-10-28 2014-07-22 Lightlab Imaging, Inc. Phase-lock loop-based clocking system, methods and apparatus
US8831321B1 (en) 2011-11-07 2014-09-09 Lightlab Imaging, Inc. Side branch detection methods, systems and devices
US20130123616A1 (en) 2011-11-16 2013-05-16 Volcano Corporation Medical Workflow System and Method
US20130281832A1 (en) 2012-04-24 2013-10-24 John Baumgart System for Coregistration of Optical Coherence Tomography and Angiographic X-ray Image Data
WO2013175472A2 (en) 2012-05-21 2013-11-28 Sync-Rx, Ltd. Co-use of endoluminal data and extraluminal imaging
WO2014002095A2 (en) 2012-06-26 2014-01-03 Sync-Rx, Ltd. Flow-related image processing in luminal organs
US20140100451A1 (en) 2012-06-26 2014-04-10 Sync-Rx, Ltd. Coregistration of endoluminal data points with values of a luminal-flow-related index
US20140107479A1 (en) 2012-06-26 2014-04-17 Sync-Rx, Ltd. Determining a luminal-flow-related index of a lumen by performing image processing on two-dimensional images of the lumen
US20140114184A1 (en) 2012-06-26 2014-04-24 Sync-Rx, Ltd. Determining a luminal-flow-related index using blood velocity determination
US20140114185A1 (en) 2012-06-26 2014-04-24 Sync-Rx, Ltd. Determining a characteristic of a lumen by measuring temporal changes in contrast agent density
US20150141808A1 (en) * 2012-06-28 2015-05-21 Koninklijke Philips N.V. Fiber optic sensor guided navigation for vascular visualization and monitoring
US20140024931A1 (en) 2012-07-20 2014-01-23 Lightlab Imaging, Inc. Data Encoders for Medical Devices and Related Methods
US20140218742A1 (en) 2012-08-31 2014-08-07 Lightlab Imaging, Inc. Optical Coherence Tomography Control Systems and Methods
US8687201B2 (en) 2012-08-31 2014-04-01 Lightlab Imaging, Inc. Optical coherence tomography control systems and methods
US20140142427A1 (en) 2012-11-16 2014-05-22 Lightlab Imaging, Inc. Automated Fluid Delivery Catheter and System
US20140142432A1 (en) 2012-11-19 2014-05-22 Christopher Hutchins Multimodal Imaging Systems, Probes and Methods
US20140142436A1 (en) 2012-11-19 2014-05-22 Christopher Hutchins Interface Devices, Systems and Methods for Multimodal Probes
US8913084B2 (en) 2012-12-21 2014-12-16 Volcano Corporation Method and apparatus for performing virtual pullback of an intravascular imaging device
US20140187920A1 (en) 2012-12-31 2014-07-03 Volcano Corporation Devices, Systems, and Methods For Assessment of Vessels
US20140270445A1 (en) 2013-03-13 2014-09-18 Volcano Corporation System and method for oct depth calibration
US20140268167A1 (en) 2013-03-15 2014-09-18 Lightlab Imaging, Inc. Calibration and Image Processing Devices, Methods, and Systems

Non-Patent Citations (14)

* Cited by examiner, † Cited by third party
Title
Annex to Form PCT/ISA206 Communication Relating to the Results of the Partial International Search for International Application No. PCT/US2008/012701, dated Feb. 27, 2009 (3 pages).
Dave Fornell, "The Advantages and Disadvantages of OCT vs. IVUS", Diagnostic and Interventional Cardiology, May 18, 2011, pp. 1-4.
International Preliminary Report on Patentability for International application No. PCT/US2015/042849 issued from the International Bureau of WIPO dated Mar. 14, 2017 (11 pages).
International Search Report and Written Opinion mailed from the International Searching Authority dated Jun. 27, 2014 for International Application No. PCT/US2013/030623 (17 pages).
International Search Report and Written Opinion of the International Searching Authority for International Application No. PCT/US2015/042849 mailed from the International Searching Authority dated Nov. 2, 2015 (16 pages).
International Search Report for International Application No. PCT/US2008/012701, dated May 14, 2009 (7 pages).
JP 2017-534518, Notification of Reason(s) for Refusal, dated May 14, 2019, (5 pages).
Palti-Wasserman et al., "Identifying and Tracking a Guide Wire in the Coronary Arteries During Angioplasty from X-Ray Images", IEEE transactions on biomedical engineering, 44:2, Feb. 1997, pp. 152-164.
PCT International Preliminary Report on Patentability for International Application No. PCT/US2008/012701, dated May 18, 2010 (10 pages).
PCT International Search Report and Written Opinion of International Searching Authority for International Application No. PCT/US2013/078500, dated Jul. 8, 2014 (14 pages).
Perez-Rovira et al., "Deformable Registration of Retinal Fluorescein Angiogram Sequences Using Vasculature Structures", 32nd Annual Conf. of IEEE EMBS, 2010, pp. 4383-4386.
Shengxian Tu et al., "In vivo comparison of arterial lumen dimensions assessed by co-registered three-dimensional (3D) quantitative coronary angiography, intravascular ultrasound and optical coherence tomography", Int. J. Cardiovasc Imaging (2012) 28:1315-1327.
Tung et al., "Automatic Detection of Coronary Stent Struts in Intravascular OCT Imaging", Proceedings of SPIE, vol. 8315, Feb. 22, 2012 (8 pages).
Written Opinion of the International Searching Authority for International Application No. PCT/US2008/012701, dated May 14, 2009 (10 pages).

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11278206B2 (en) 2015-04-16 2022-03-22 Gentuity, Llc Micro-optic probes for neurology
US11064873B2 (en) 2015-08-31 2021-07-20 Gentuity, Llc Imaging system includes imaging probe and delivery devices
US11583172B2 (en) 2015-08-31 2023-02-21 Gentuity, Llc Imaging system includes imaging probe and delivery devices
US11937786B2 (en) 2015-08-31 2024-03-26 Gentuity, Llc Imaging system includes imaging probe and delivery devices
US20190154595A1 (en) * 2016-05-20 2019-05-23 Perimeter Medical Imaging, Inc. Method and system for combining microscopic imaging with x-ray
US11058388B2 (en) * 2016-05-20 2021-07-13 Perimeter Medical Imaging, Inc. Method and system for combining microscopic imaging with X-Ray imaging
US11684242B2 (en) 2017-11-28 2023-06-27 Gentuity, Llc Imaging system
US11344373B2 (en) 2018-05-29 2022-05-31 Lightlab Imaging, Inc. Stent expansion display, systems, and methods

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